Supresa® (Saffron Extract for Appetite & Crave Control — PLT Health)

Crocus sativus
Evidence Level
Limited
3 Clinical Trials
5 Documented Benefits
2/5 Evidence Score

Supresa is the North American trade name, marketed by PLT Health Solutions, for the saffron (Crocus sativus L.) stigma extract that its French developer Inoreal also sells as Satiereal; Inoreal owns both trademarks. Its own evidence is a single 8-week randomized, placebo-controlled trial in 60 mildly overweight women taking 176.5 mg/day, which reported fewer snacking episodes and a statistically significant body-weight difference versus placebo, while other body measurements and vital signs were almost unchanged, so the difference was small. The developer attributes the effect to serotonin and mood, but the published abstract reports no mood or serotonin measurements. A small 28-day university trial that gave the extract inside a combination supplement found no significant difference from placebo in weight, cravings, hunger or mood, and a pooled analysis of 25 saffron trials in overweight adults found no significant effect on body weight or BMI. Saffron is listed as generally recognized as safe for its intended use under 21 CFR 182.20, which covers food use, not a review of supplemental doses. Studied dose: 176.5 mg/day.

Studied Dose 176.5 mg/day, taken as one 88.25 mg capsule twice daily, the dose in the single 8-week trial of this extract. A 28-day trial gave 178 mg/day inside a combination supplement. Saffron mood trials of other preparations use about 30 mg/day, which is not evidence for this dose.
Active Compound Saffron (Crocus sativus L.) stigma extract, the same material sold as Satiereal. PLT Health states it is standardized to more than 0.3% safranal and rich in safranal, crocin and picrocrocin, and retail labels of the extract under its Satiereal name state 0.3% safranal; no numeric specification for crocin or picrocrocin was found.

Benefits

Snacking and satiety: fewer snacking episodes than placebo

In one 8-week randomized, placebo-controlled trial in 60 mildly overweight women, self-recorded snacking frequency fell significantly more on 176.5 mg/day than on placebo (P < .05). PLT Health reports a 55% drop on the extract against 28% on placebo, so placebo improved substantially too; those percentages are not in the published abstract. This single trial has not been independently replicated.

Appetite: company-reported decrease, mixed in other saffron trials

PLT Health states that self-reported appetite in this single trial fell 69% on the extract against 54% on placebo, while a trade report on the developer's patent gave 84% against 52%; neither figure is in the published abstract. Other saffron preparations are mixed: 30 mg/day did not reduce food craving and 100 mg/day did not change appetite, while 30 mg/day in heart patients lowered appetite within the saffron group.

Studied only in mildly overweight women, for 8 weeks

The published trial enrolled 60 healthy, mildly overweight women, so it says nothing about men, people at a higher BMI, or use beyond 8 weeks. A PLT Health sales sheet says effects began within 14 days and reached up to 3 times placebo in women considered snackers; that subgroup result is not reported in the published abstract and should not be treated as demonstrated.

Mood and stress-eating rationale: untested for this extract

The developer's rationale is that saffron improves mood and so reduces stress-driven snacking. The published abstract of the 8-week trial reports no mood or stress measurements, so for this extract that remains a hypothesis. A 28-day randomized trial that gave 178 mg of the extract inside a supplement with naringin and vitamin D3 found no difference from placebo in mood states, cravings, anxiety or stress.

Body weight: small difference in one trial, not confirmed elsewhere

In the single 8-week trial the extract group lost significantly more weight than placebo (P < .01), but other body measurements and vital signs were almost unchanged, so the difference was small. A pooled analysis of 25 randomized saffron trials in overweight and obese adults found no significant effect on body weight or BMI, and the 28-day combination trial found no change in body mass, BMI or waist size.

Mechanism of action

1

Proposed serotonergic activity

PLT Health describes the extract as acting by enhancing serotonin, and the trial authors proposed that a mood-improving effect would reduce snacking. Serotonin signalling is involved in mood and in satiety, which is the basis for the idea that the extract acts on mood-driven eating rather than on metabolism. Serotonin has not been measured in people taking this extract, so this remains a proposed route.

2

Stress-related snacking hypothesis

The trial authors note that snacking is frequently associated with stress, and hypothesized that the extract would reduce snacking through its suggested mood-improving effect. Stress, cortisol and craving are not reported outcomes of that trial, and a 28-day trial that gave the extract inside a combination supplement found no difference from placebo in stress, anxiety or food cravings.

3

Proposed satiety signalling

Serotonin is one of the signals involved in feelings of fullness, and the proposal is that supporting it nudges satiety rather than blunting hunger with a stimulant. Satiety hormones such as GLP-1 and objectively measured food intake are not reported outcomes in the trials of this extract, so this remains a proposed route, and no data show that this extract acts on GLP-1.

4

Saffron compounds and standardization

Safranal, crocins and picrocrocin are characteristic saffron compounds. Retail labels for this extract state standardization to 0.3% safranal. How much each compound contributes to the reported effects has not been tested, and no head-to-head trial has compared this extract with other saffron extracts.

5

Non-stimulant profile

The extract is not a stimulant and is not proposed to act through central nervous system stimulation. In the 8-week trial vital signs were almost unchanged and no participant withdrew because of the product. Safety beyond 8 weeks has not been studied, so suitability for long-term daily use is not established.

Clinical trials

1
Supresa (as Satiereal) 8-Week Snacking and Body-Weight Trial in Women
PubMed

Randomized, double-blind, placebo-controlled trial of 176.5 mg/day of this saffron stigma extract (one capsule twice daily) versus placebo for 8 weeks, published as Gout B, Bourges C, Paineau-Dubreuil S, Nutrition Research 2010;30(5):305-13, under the extract's other brand name, Satiereal (Inoreal). PLT Health publishes the same study as its Supresa trial. Primary outcome was body weight; the main secondary outcome was snacking frequency, self-recorded in a nutrition diary. Caloric intake was not restricted. The abstract does not state funding.

Sixty healthy, mildly overweight women (PLT Health gives a BMI range of 25 to 30 and ages 25 to 45); 31 on the extract and 29 on placebo, over 8 weeks.

Body weight fell significantly more on the extract than on placebo (P < .01) and snacking frequency fell significantly more (P < .05). Other anthropometric measures and vital signs remained almost unchanged in both groups, so the weight difference was small. PLT Health's figures for the same trial are a 55% versus 28% drop in snacking and a 69% versus 54% decrease in appetite (a trade report on the developer's patent gave 84% versus 52%); these are not in the published abstract. No participant withdrew because of the product. The abstract reports no mood or stress outcomes. One small trial, not independently replicated.

2
Satiereal, Naringin and Vitamin D3 Combination: 28-Day Trial in Overweight Adults
PubMed

Randomized, double-blind, placebo-controlled trial at Hofstra University of a multi-ingredient supplement containing 178 mg Satiereal (the same saffron extract sold as Supresa), 100 mg naringin and 2,000 IU vitamin D3 daily for 28 days. Published as Gonzalez AM, Sell KM, Ghigiarelli JJ, Spitz RW, Accetta MR, Mangine GT, Journal of Dietary Supplements 2018;15(6):965-76. Measures included body mass, BMI, waist circumference, self-reported food records, Profile of Mood States, visual analog scales and food-craving questionnaires.

Twenty healthy overweight adults (mean age 25.5, mean BMI 29.9), ten on the supplement and ten on placebo, over 28 days.

No significant difference between groups in total calorie or macronutrient intake, body mass, BMI or waist circumference, and no difference in mood states, food cravings, anxiety, fullness, bloating, hunger or stress. The authors concluded the supplement had no detectable beneficial effect on body-weight management. The study was small (20 people) and short (28 days), so it could miss a modest effect, and the saffron extract was given with other ingredients, so the result is for the combination, not the extract alone.

3
Saffron Meta-Analysis: Body Weight and Cardiometabolic Measures in Overweight Adults
PubMed

Systematic review and meta-analysis of 25 randomized controlled trials of saffron in overweight and obese patients, published as Tahmasbi F, Araj-Khodaei M, Mahmoodpoor A, Sanaie S, Phytotherapy Research 2022;36(9):3394-3414. This is an evidence synthesis of various saffron preparations and doses, not a trial of this specific extract.

Overweight and obese adults pooled across 25 randomized trials of various saffron preparations.

Pooling the trials showed no significant effect of saffron on body weight (-0.32 kg; CI -3.15 to 2.51; p = 0.82), BMI (-0.06 kg/m2; CI -1.04 to 0.93; p = 0.91), waist circumference (p = 0.41) or hip circumference (p = 0.89). Waist-to-hip ratio fell significantly (SMD -0.41; CI -0.73 to -0.09; p = 0.01). The authors described promising effects on some cardiometabolic factors, noted limitations mainly from heterogeneity among the included studies, and called for higher-quality evidence.

Side effects and drug interactions

Common Potential side effects

In the 8-week trial of this extract no participant withdrew because of the product and vital signs were almost unchanged.
Saffron is listed under 21 CFR 182.20 among natural extractives generally recognized as safe for their intended use in food; that listing is not a safety review of a 176.5 mg/day supplemental dose.
Bloating did not differ from placebo in a 28-day trial of a combination supplement containing this extract.
A review reports very few adverse health effects of saffron, but advises avoiding high doses (more than 5 g/day) in pregnancy because of uterine-stimulating activity; supplemental doses have not been tested in pregnancy or lactation.
Long-term safety at supplemental doses is not established; the longest trial of this extract ran 8 weeks.

Important Drug interactions

SSRI and SNRI antidepressants (sertraline, fluoxetine, venlafaxine, etc.): saffron is proposed to act on serotonin, so there is a theoretical risk of additive serotonergic effects; talk to your prescriber before combining.
MAO inhibitors: theoretical additive serotonergic risk; consult your prescriber.
Triptan migraine medications: theoretical additive serotonergic risk; consult your prescriber.
Lithium: theoretical interaction through serotonergic effects; consult your prescriber.
GLP-1 agonist medications (Ozempic, Wegovy, Mounjaro): no interaction is known, and the combination has not been studied; talk to your prescriber before adding anything to a prescribed weight-loss regimen.
Other weight-loss medications: not studied together; consult your prescriber before combining.

Frequently asked questions about Supresa® (Saffron Extract for Appetite & Crave Control — PLT Health)

What is Supresa?

Supresa is the North American trade name, marketed by PLT Health Solutions, for the saffron (Crocus sativus L.) stigma extract that its French developer Inoreal also sells as Satiereal; Inoreal owns both trademarks.

What is Supresa used for?

Supresa is researched primarily for Weight Management. In one 8-week randomized, placebo-controlled trial in 60 mildly overweight women, self-recorded snacking frequency fell significantly more on 176.5 mg/day than on placebo (P < .05).

What is the recommended dosage of Supresa?

The clinically studied dose is 176.5 mg/day, taken as one 88.25 mg capsule twice daily, the dose in the single 8-week trial of this extract. A 28-day trial gave 178 mg/day inside a combination supplement. Always follow the product label and check with a healthcare provider for personal advice.

Is Supresa safe, and does it have side effects?

Side effects and cautions reported for Supresa include: In the 8-week trial of this extract no participant withdrew because of the product and vital signs were almost unchanged. Saffron is listed under 21 CFR 182. It may also interact with some medications. Supresa is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Supresa interact with any medications?

Possible interactions include: SSRI and SNRI antidepressants (sertraline, fluoxetine, venlafaxine, etc.): saffron is proposed to act on serotonin, so there is a theoretical risk of additive serotonergic effects; talk to your prescriber before combining. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Supresa?

NutraSmarts rates the evidence for Supresa as Limited (2 out of 5). It is backed by 3 study summaries and 7 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(7 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Akhondzadeh S, Mostafavi SA, Keshavarz SA, Mohammadi MR, Hosseini S, Eshraghian MR. A placebo controlled randomized clinical trial of Crocus sativus L. (saffron) on depression and food craving among overweight women with mild to moderate depression. J Clin Pharm Ther. 2020;45(1):134-143. doi: 10.1111/jcpt.13040.PubMedUsed to support: Twelve-week randomized, double-blind, placebo-controlled trial of 30 mg/day saffron (15 mg twice daily) in overweight women with mild-to-moderate depression: 73 randomized, 52 completed. Depression scores fell significantly more than placebo (-8.4 vs -3.9 points; P = .007), but there was no significant effect on food craving (F(1,29) = 0.38, P = .54), and the authors concluded that saffron capsules were not effective in reducing food craving. It used a different, generic saffron preparation at about one-sixth of the dose on this page.
  2. Ahmadikhatir S, Ostadrahimi A, Safaiyan A, Ahmadikhatir S, Farrin N. Saffron (Crocus sativus L.) supplements improve quality of life and appetite in atherosclerosis patients: A randomized clinical trial. J Res Med Sci. 2022;27:30. doi: 10.4103/jrms.JRMS_1253_20.PubMedUsed to support: Six-week randomized, double-blind, placebo-controlled trial of 100 mg/day saffron in 63 patients with atherosclerosis. The physical (p = 0.008) and social (p = 0.012) domains of quality of life improved versus placebo, but despite the paper's title the abstract states that saffron did not significantly affect appetite levels or the emotional domain of quality of life. A different dose, a different preparation and a cardiac-patient population, and it does not support an appetite effect.
  3. Tahmasbi F, Araj-Khodaei M, Mahmoodpoor A, Sanaie S. Effects of saffron (Crocus sativus L.) on anthropometric and cardiometabolic indices in overweight and obese patients: A systematic review and meta-analysis of randomized controlled trials. Phytother Res. 2022;36(9):3394-3414. doi: 10.1002/ptr.7530.PubMedUsed to support: Systematic review and meta-analysis of 25 randomized controlled trials of saffron in overweight and obese patients. Pooling the trials found no significant effect on body weight (-0.32 kg; CI -3.15 to 2.51; p = 0.82), BMI (-0.06 kg/m2; CI -1.04 to 0.93; p = 0.91), waist circumference (p = 0.41) or hip circumference (p = 0.89); waist-to-hip ratio fell significantly (SMD -0.41; CI -0.73 to -0.09; p = 0.01). The authors described promising effects on some cardiometabolic factors, noted limitations mainly from heterogeneity, and called for higher-quality evidence. It pools various saffron preparations and doses, not this extract.
  4. Gout B, Bourges C, Paineau-Dubreuil S. Satiereal, a Crocus sativus L extract, reduces snacking and increases satiety in a randomized placebo-controlled study of mildly overweight, healthy women. Nutr Res. 2010;30(5):305-13. doi: 10.1016/j.nutres.2010.04.008.PubMedUsed to support: The single published trial of this extract, run under its other brand name, Satiereal (PLT Health presents the same study as its Supresa trial): 60 healthy, mildly overweight women took 176.5 mg/day, as one capsule twice daily, or placebo for 8 weeks with no calorie restriction. Body weight fell significantly more than on placebo (P < .01) and self-recorded snacking frequency fell significantly more (P < .05), while other anthropometric measures and vital signs remained almost unchanged and no participant withdrew because of the product. Small (n=60), 8 weeks, not independently replicated; the abstract reports no mood or stress outcomes and does not state funding.
  5. Gonzalez AM, Sell KM, Ghigiarelli JJ, Spitz RW, Accetta MR, Mangine GT. Effect of Multi-Ingredient Supplement Containing Satiereal, Naringin, and Vitamin D on Body Composition, Mood, and Satiety in Overweight Adults. J Diet Suppl. 2018;15(6):965-976. doi: 10.1080/19390211.2017.1407385.PubMedUsed to support: University-run (Hofstra University) 28-day randomized, double-blind, placebo-controlled trial in 20 overweight adults of a supplement containing 178 mg Satiereal (the same extract sold as Supresa) with 100 mg naringin and 2,000 IU vitamin D3. There was no significant difference from placebo in calorie or macronutrient intake, body mass, BMI or waist circumference, and none in mood states, food cravings, hunger, fullness, bloating, anxiety or stress; the authors concluded it had no detectable beneficial effect on body-weight management. Small (n=20), short (28 days), and a combination product rather than the extract alone.
  6. Poma A, Fontecchio G, Carlucci G, Chichiriccò G. Anti-inflammatory properties of drugs from saffron crocus. Antiinflamm Antiallergy Agents Med Chem. 2012;11(1):37-51. doi: 10.2174/187152312803476282.PubMedUsed to support: Narrative review of saffron constituents and their proposed uses. It states that very few adverse health effects of saffron have been demonstrated and that high doses (more than 5 g/day) should be avoided in pregnancy because of uterine-stimulating activity. Cited here only for the pregnancy caution; it is not evidence for this extract's effects.
  7. Abedimanesh N, Bathaie SZ, Abedimanesh S, Motlagh B, Separham A, Ostadrahimi A. Saffron and crocin improved appetite, dietary intakes and body composition in patients with coronary artery disease. J Cardiovasc Thorac Res. 2017;9(4):200-208. doi: 10.15171/jcvtr.2017.35.PubMedUsed to support: 8-week randomized, double-blind, placebo-controlled trial in 84 adults aged 40 to 65 with coronary artery disease: 30 mg/day saffron aqueous extract, 30 mg/day crocin or placebo. Appetite decreased significantly within the saffron group (P < 0.001) and the crocin group (P = 0.029). A different saffron preparation and population, not this extract; backs the 'mixed in other saffron trials' appetite statement.