Aspurūs™ (Shatavari for Menopause)

Asparagus racemosus Willd.
Evidence Level
Limited
2 Clinical Trials
5 Documented Benefits
2/5 Evidence Score

Standardized full-spectrum Shatavari root extract (5% Shatavarins) developed for menopause. In a 70-person randomized, double-blind, placebo-controlled trial, a shatavari root extract improved hot flashes, night sweats, insomnia, anxiety, vaginal dryness, libido and quality of life compared with placebo. That published report does not name a branded extract, so the findings belong to shatavari root extract generally rather than to this brand specifically.

Studied Dose 300 mg once daily for 8 weeks (the only dose stated in any cited published trial).
Active Compound Shatavarins (steroidal saponins, standardized to 5% in Aspurūs™), racemofuran, asparagamine A, isoflavones, polysaccharides, flavonoids.

Benefits

Reduced hot flashes and night sweats

In a 70-person double-blind, placebo-controlled trial in peri- and postmenopausal women (Gudise 2024), the shatavari group had significantly fewer hot flashes and night sweats than the placebo group. A separate 8-week trial in 80 perimenopausal women (73 completed) using 300 mg of shatavari root extract once daily also reported improvement in hot flashes versus placebo (p=0.002). Both trials are small, and the published report of the 70-person trial does not name a branded extract.

Improved sleep and reduced insomnia

In the 70-person Gudise 2024 trial, women taking shatavari reported less insomnia than those taking placebo. This rests on one small trial, so treat it as early rather than settled evidence.

Anxiety, nervousness, and mood symptom relief

In the 70-person Gudise 2024 trial, anxiety and nervousness improved more than with placebo. In a separate 8-week trial in 135 women aged 45 to 65, mood improved (p=0.008) and esteem-related affect improved (p=0.025) between groups. That trial had both a shatavari-alone arm and an ashwagandha-plus-shatavari arm, so any result from the combination arm cannot be credited to shatavari on its own.

Vaginal dryness and libido improvement

The 70-person Gudise 2024 trial reported greater improvement in vaginal dryness and libido than placebo. This comes from that single small trial. How it works is not established; researchers have proposed mild plant-estrogen activity combined with effects on the stress response.

Quality of life improvement

Utian Quality of Life scores improved significantly versus placebo in the 70-person Gudise 2024 trial. In the 135-woman trial, MENQOL (Menopause-Specific Quality of Life Questionnaire) scores improved numerically by week 8, meaning the change went in the expected direction but was not reported as statistically significant.

Mechanism of action

1

Phytoestrogenic activity of Shatavarins

Shatavarin saponins have a steroidal structure resembling endogenous estrogens and bind weakly to estrogen receptors. This weak, SERM-like binding is the leading explanation for symptom relief, but it is a proposal rather than something the human trials tested. It should not be read as proof of safety: one of the cited trials measured changes in estradiol, FSH and T3, so anyone with a hormone-sensitive condition should speak to a doctor first.

2

Adaptogenic HPA-axis modulation

Shatavari is classified as a rasayana in Ayurveda — a category overlapping with the modern adaptogen concept. Animal studies show effects on the hypothalamic-pituitary-adrenal stress axis and a reduced cortisol response to stress. Whether this explains the anxiety and sleep changes seen in people has not been tested, because the human trials did not measure it.

3

GABAergic and 5-HT receptor effects

Preclinical work has identified GABAergic activity and serotonergic receptor modulation by Shatavari extracts — mechanisms that could contribute to anxiolytic and sleep-promoting effects. This is all laboratory and animal research, and no human trial of shatavari has measured these pathways, so it remains a hypothesis.

4

Antioxidant and anti-inflammatory activity

Asparagus racemosus root contains saponins, isoflavones, and polysaccharides with documented antioxidant activity. That activity has been measured in the laboratory, not in people. None of the human trials cited here measured oxidative stress or any healthy-aging outcome, so this is background chemistry rather than a demonstrated benefit.

Clinical trials

1
Aspurūs™ Multicenter Menopause Clinical Trial

Double-blind, multicenter, randomized, placebo-controlled clinical trial (Gudise VS, Dasari MP, Kuricheti SSK 2024, Cureus 16(4):e57879, doi:10.7759/cureus.57879). Important limitation: the published report does not name a branded extract. It refers only to the test group and the test compound, and identifies the plant only as Asparagus racemosus. No trademark, no standardization percentage and no dose appear in it. The listed affiliations are two Indian hospitals and an Ayurveda practice, with no company named and no funding statement, so who funded the trial is not stated.

70 peri- and postmenopausal women with menopausal symptoms (hot flashes, night sweats, anxiety, fatigue, depression, insomnia, mood swings), randomized to two groups of 35: shatavari root extract or a microcrystalline cellulose placebo. Thirty-five people per group is a small trial.

The shatavari group improved more than placebo in hot flashes, night sweats, insomnia, anxiety, nervousness, vaginal dryness and loss of libido, and Utian Quality of Life scores improved significantly. No significant adverse events were recorded. The authors' own wording was that the test compound could be a safe alternative to modern drugs. No trial cited here compared shatavari with hormone replacement therapy, so nothing in this research shows it can stand in for HRT; that decision belongs with your doctor.

2
Shatavari + Ashwagandha 3-Arm Clinical Trial

8-week, randomized, double-blind, placebo-controlled, multicentric study (Ademola, Ajgaonkar, Debnath, Debnath, Frontiers in Reproductive Health, doi:10.3389/frph.2025.1654503).

135 women aged 45 to 65 with menopausal symptoms, randomized to three groups for 8 weeks: shatavari root extract alone, an ashwagandha plus shatavari combination, or placebo. The published report does not state the dose used; among the trials cited here, only the perimenopause study states a dose (300 mg once daily).

MRS (Menopause Rating Scale) scores improved at weeks 4 and 8. Esteem-related affect improved (p=0.025) and mood improved significantly (p=0.008) between groups. MENQOL scores improved numerically by week 8. This trial reported that hormone levels stayed within normal limits. That is not the whole picture: a third cited trial in perimenopausal women (Mahajan 2025) reported measurable changes in estradiol (p=0.003), FSH (p=0.028) and T3 (p=0.021), so shatavari should not be described as having no hormonal effect. Mild adverse events reported in 4 participants (loose stools, dizziness, nausea, headache). The authors concluded that the ashwagandha plus shatavari combination is a promising option for managing menopausal symptoms; that conclusion is about the combination, not about shatavari on its own.

Side effects and drug interactions

Common Potential side effects

Generally well tolerated in the short trials done so far: the 70-person trial recorded no significant adverse events and the 135-woman trial recorded only mild ones. These trials were short (the two that state a duration ran 8 weeks), so longer-term safety is unknown.
Mild GI symptoms (loose stools, nausea) reported infrequently in Ademola 2025.
Asparagus allergy is a contraindication — Shatavari is closely related to edible asparagus and cross-reactivity is possible.
Shatavari has mild plant-estrogen activity, and the Mahajan 2025 perimenopause trial measured a rise in estradiol. If you have a personal or family history of breast, ovarian or uterine cancer, or endometriosis or fibroids, talk to your doctor before using it.
Theoretical: diuretic effect at high doses; stay well hydrated. Menopausal symptoms, and especially any unusual or unexpected vaginal bleeding, should be assessed by a doctor rather than self-treated.

Important Drug interactions

Tamoxifen, aromatase inhibitors, and other anti-estrogenic agents — theoretical interaction; avoid in breast cancer patients without oncologist approval.
Diuretics — additive effect possible.
Lithium — diuretic effect could theoretically affect lithium clearance.
Hormone replacement therapy — overlap with conventional HRT not well-studied; combining is not recommended without provider supervision.
Diabetes medications, mild blood-sugar-lowering effects have been reported for shatavari, but not in the human menopause trials cited here. If you take glucose-lowering medication, monitor your blood sugar and tell your doctor.

Frequently asked questions about Aspurūs™ (Shatavari for Menopause)

What is Aspurūs?

Standardized full-spectrum Shatavari root extract (5% Shatavarins) developed for menopause. In a 70-person randomized, double-blind, placebo-controlled trial, a shatavari root extract improved hot flashes, night sweats, insomnia, anxiety, vaginal dryness, libido and quality of life compared with placebo.

What is Aspurūs used for?

Aspurūs is researched primarily for Menopause Support and Women's Health. In a 70-person double-blind, placebo-controlled trial in peri- and postmenopausal women (Gudise 2024), the shatavari group had significantly fewer hot flashes and night sweats than the placebo group.

What is the recommended dosage of Aspurūs?

The clinically studied dose is 300 mg once daily for 8 weeks (the only dose stated in any cited published trial). Always follow the product label and check with a healthcare provider for personal advice.

Is Aspurūs safe, and does it have side effects?

For most healthy adults, Aspurūs is well tolerated at studied doses. Reported effects can include: Generally well tolerated in the short trials done so far: the 70-person trial recorded no significant adverse events and the 135-woman trial recorded only mild ones. These trials were short (the two that state a duration ran 8 weeks), so longer-term safety is unknown. It may also interact with some medications. Aspurūs 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 Aspurūs interact with any medications?

Possible interactions include: Tamoxifen, aromatase inhibitors, and other anti-estrogenic agents — theoretical interaction; avoid in breast cancer patients without oncologist approval. Diuretics — additive effect possible. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Aspurūs?

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

References(3 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. Ademola J, Ajgaonkar A, Debnath T, Debnath K, Langade J Efficacy and safety of Shatavari root extract (Asparagus racemosus) for menopausal symptoms: a randomized, double-blind, three-arm, placebo-controlled study Frontiers in Reproductive Health. 2025;7:1654503. doi:10.3389/frph.2025.1654503.PubMedUsed to support: Three-arm double-blind placebo-controlled trial in 135 women aged 45 to 65 over 8 weeks. Menopause Rating Scale scores improved at weeks 4 and 8, mood improved (p=0.008) and esteem-related affect improved (p=0.025). One arm took shatavari alone and one took ashwagandha plus shatavari, so results from the combination arm do not support shatavari by itself. The report does not state a dose, and it does not support every benefit listed on this page.
  2. Gudise VS, Dasari MP, Kuricheti SSK Efficacy and Safety of Shatavari Root Extract for the Management of Menopausal Symptoms: A Double-Blind, Multicenter, Randomized Controlled Trial Cureus. 2024;16(4):e57879. doi:10.7759/cureus.57879.PubMedUsed to support: Multicenter double-blind placebo-controlled trial in 70 women (35 per group) reporting improvement in hot flashes, night sweats, insomnia, anxiety, nervousness, vaginal dryness and libido, plus Utian Quality of Life scores, with no significant adverse events. The published report names no brand, no standardization figure and no dose, and the trial is small.
  3. Mahajan S, Avad P, Langade J Efficacy and Safety of Shatavari (Asparagus racemosus) Root Extract for Perimenopause: Randomized, Double-Blind, Placebo-Controlled Study International Journal of Women's Health. 2025;17:4057-4073. doi:10.2147/IJWH.S544267.PubMedUsed to support: Double-blind placebo-controlled trial in perimenopausal women: 80 randomized, 73 completed, shatavari root extract 300 mg once daily for 8 weeks. Menopause Rating Scale scores improved (p<0.0001), perceived stress improved (p<0.0001) and hot flashes improved (p=0.002). This trial also measured changes in estradiol (p=0.003), FSH (p=0.028) and T3 (p=0.021). It is the only cited trial that states a dose.