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. Multicenter RCT showed improvements in hot flashes, night sweats, insomnia, anxiety, vaginal dryness, libido, and quality of life vs placebo.

Studied Dose Aspurūs™ proprietary dose used in Gudise 2024 multicenter RCT was administered to peri-/post-menopausal women aged 40-65 years over the trial duration. The Ademola 2025 three-arm RCT used 300 mg/day Shatavari root extract for 8 weeks. Traditional Ayurvedic dosing for general use is 1-3 g of root powder/day, but standardized extracts achieve effects at 300-500 mg/day due to concentration of Shatavarin saponins.
Active Compound Shatavarins (steroidal saponins, standardized to 5% in Aspurūs™), racemofuran, asparagamine A, isoflavones, polysaccharides, flavonoids

Benefits

Reduced hot flashes and night sweats

Gudise 2024 (multicenter RCT, peri/postmenopausal women) showed Aspurūs™ produced positive and significant reduction in hot flashes and night sweats vs placebo. Manufacturer reports support 85% reduction in hot flashes within 4 weeks and 90% reduction in night sweats within 8 weeks in their internal trial data.

Improved sleep and reduced insomnia

Gudise 2024 found significant improvement in Regensburg Insomnia Scale scores in the Shatavari group. Manufacturer data references 60% reduction in sleeplessness vs placebo. Sleep quality is one of the most disruptive menopausal symptoms — addressing it has meaningful quality-of-life impact.

Anxiety, nervousness, and mood symptom relief

Both Gudise 2024 and Ademola 2025 documented improvements in anxiety and mood-related symptoms. Ademola 2025 showed significant changes in esteem-related affect (p=0.025) and mood improvement (p=0.008) — supporting Shatavari's traditional role as both rasayana (rejuvenative) and adaptogen.

Vaginal dryness and libido improvement

Gudise 2024 reported significant reduction in vaginal dryness and improvement in libido vs placebo — symptoms often inadequately addressed by other phytoestrogen approaches. Mechanism likely combines mild phytoestrogenic activity with adaptogenic stress modulation.

Quality of life improvement

Utian QoL score improved significantly in the Shatavari group vs placebo in Gudise 2024. The MENQOL (Menopause-Specific Quality of Life Questionnaire) and POMS scores in Ademola 2025 also showed numerical improvements.

Mechanism of action

1

Phytoestrogenic activity of Shatavarins

Shatavarin saponins have a steroidal structure resembling endogenous estrogens and bind weakly to estrogen receptors. This selective estrogen receptor modulator (SERM)-like activity provides menopausal symptom relief via the estrogen pathway without the higher-affinity binding that creates cancer concerns with conventional HRT.

2

Adaptogenic HPA-axis modulation

Shatavari is classified as a rasayana in Ayurveda — a category overlapping with the modern adaptogen concept. Animal models show modulation of the hypothalamic-pituitary-adrenal axis and reduced cortisol response to stressors. This contributes to anxiety reduction and improved sleep beyond the phytoestrogen mechanism.

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. These pathways complement the phytoestrogen action and may explain why effects on mood symptoms are stronger than would be predicted from estrogen-receptor binding alone.

4

Antioxidant and anti-inflammatory activity

Asparagus racemosus root contains saponins, isoflavones, and polysaccharides with documented antioxidant activity. These reduce oxidative stress associated with the post-menopausal state, supporting a broader healthy-aging mechanism beyond direct symptom relief.

Clinical trials

1
Gudise 2024 — Aspurūs™ Multicenter Menopause RCT
PubMed

Double-blind, multicenter, randomized, placebo-controlled clinical trial (Gudise VS, Dasari MP, Kuricheti SSK 2024, Cureus 16(4):e57879, doi:10.7759/cureus.57879). The test product was Aspurūs™ — full-spectrum Asparagus racemosus root extract standardized to 5% total Shatavarins (steroidal saponins) by HPTLC.

70 peri- and postmenopausal women aged 40-65 years experiencing menopausal symptoms (hot flashes, night sweats, anxiety, fatigue, depression, insomnia, mood swings). Randomized to two groups: Aspurūs™ test group (n=35) or microcrystalline cellulose placebo (n=35).

Aspurūs™ produced positive and significant effects vs placebo in: hot flashes, night sweats, insomnia, anxiety, nervousness, vaginal dryness, and loss of libido. Utian QoL score improved significantly in the active group vs placebo. No significant adverse events recorded. Authors concluded the formulation is a safe alternative to HRT, supporting traditional Ayurvedic use of Shatavari for menopausal symptoms.

2
Ademola 2025 — Shatavari + Ashwagandha 3-Arm RCT
PubMed

8-week, randomized, double-blind, placebo-controlled, multicentric study (Ademola, Ajgaonkar, Debnath, Debnath, Langade 2025, Frontiers in Reproductive Health, doi:10.3389/frph.2025.1654503).

135 women aged 45-65 years with menopausal symptoms. Three groups: Shatavari root extract 300 mg (n=45), Ashwagandha + Shatavari combination (n=45), or placebo (n=45).

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. Normal hormonal levels were maintained — no estrogenic stimulation in pituitary-ovarian axis. Mild adverse events reported in 4 participants (loose stools, dizziness, nausea, headache). Authors concluded the Ashwagandha + Shatavari combination demonstrated a promising option for managing menopausal symptoms.

About this ingredient

About the active ingredient

Shatavari (Asparagus racemosus Willd.) — known as the 'Queen of Herbs' in Ayurveda — is a climbing plant native to India, Sri Lanka, and the Himalayas. Used for thousands of years as a women's reproductive tonic and rasayana (rejuvenative). The pharmacologically dominant compounds are Shatavarins (steroidal saponins, including shatavarin I-IV), with shatavarin IV considered the marker compound.

Other actives include racemofuran, asparagamine A, isoflavones, polysaccharides, and flavonoids. Aspurūs™ is a specific full-spectrum standardized extract developed by Waleria, manufactured to deliver 5% total Shatavarins by HPTLC quantification. The product won the 2024 NIE New Ingredient Award in the women's health category.

Aspurūs™ is allergen-free and tested for heavy metals (lead, arsenic, cadmium, mercury) per AOAC 2015.01 methodology. EVIDENCE: Gudise 2024 multicenter RCT (Aspurūs™-specific) is the strongest brand-specific evidence — a placebo-controlled trial showing meaningful improvements across hot flashes, night sweats, anxiety, insomnia, vaginal dryness, libido, and QoL. Ademola 2025 (300 mg generic Shatavari extract, 3-arm RCT, n=135) provides confirmatory evidence with the unique three-arm design comparing Shatavari alone, Shatavari + Ashwagandha, and placebo.

2/5 evidence rating reflects: only 2 RCTs at this point, both manufacturer-affiliated, with relatively short durations; broader use cases (women's reproductive health, lactation support) rest on traditional use rather than RCT validation. SAFETY: Excellent safety record over centuries of Ayurvedic use and confirmed in modern trials. Asparagus allergy and estrogen-sensitive conditions are the main contraindications.

Best positioned as a non-hormonal alternative for women who cannot or prefer not to use HRT — set realistic expectations: effects emerge over 4-8 weeks and are most pronounced for vasomotor symptoms, mood, and sleep.

Side effects and drug interactions

Common Potential side effects

Generally well-tolerated; both pivotal trials reported no serious adverse events.
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.
Theoretical concern in estrogen-sensitive conditions (breast cancer history, endometrial cancer, fibroids) due to phytoestrogenic activity — though the Ademola 2025 trial documented unchanged hormonal parameters.
Theoretical: diuretic effect at high doses; stay well-hydrated.

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 — Shatavari has shown mild hypoglycemic effects in some studies; monitor blood glucose in diabetics.

Frequently asked questions about Aspurūs™ (Shatavari for Menopause)

What is the recommended dosage of Aspurūs™ (Shatavari for Menopause)?

The clinically studied dose for Aspurūs™ (Shatavari for Menopause) is Aspurūs™ proprietary dose used in Gudise 2024 multicenter RCT was administered to peri-/post-menopausal women aged 40-65 years over the trial duration. The Ademola 2025 three-arm RCT used 300 mg/day Shatavari root extract for 8 weeks. Traditional Ayurvedic dosing for general use is 1-3 g of root powder/day, but standardized extracts achieve effects at 300-500 mg/day due to concentration of Shatavarin saponins.. Always follow product labeling and consult a healthcare provider for personalized dosing recommendations.

What is Aspurūs™ (Shatavari for Menopause) used for?

Aspurūs™ (Shatavari for Menopause) is studied for reduced hot flashes and night sweats, improved sleep and reduced insomnia, anxiety, nervousness, and mood symptom relief. Gudise 2024 (multicenter RCT, peri/postmenopausal women) showed Aspurūs™ produced positive and significant reduction in hot flashes and night sweats vs placebo.

Are there side effects from taking Aspurūs™ (Shatavari for Menopause)?

Reported potential side effects may include: Generally well-tolerated; both pivotal trials reported no serious adverse events. Mild GI symptoms (loose stools, nausea) reported infrequently in Ademola 2025. Always consult a healthcare provider before starting any new supplement, especially if you have underlying conditions or take medications.

Does Aspurūs™ (Shatavari for Menopause) interact with medications?

Known drug interactions may include: Tamoxifen, aromatase inhibitors, and other anti-estrogenic agents — theoretical interaction; avoid in breast cancer patients without oncologist approval. Diuretics — additive effect possible. Consult a pharmacist or healthcare provider if you take prescription medications.

Is Aspurūs™ (Shatavari for Menopause) good for menopause support?

Yes, Aspurūs™ (Shatavari for Menopause) is researched for Menopause Support support. Utian QoL score improved significantly in the Shatavari group vs placebo in Gudise 2024. The MENQOL (Menopause-Specific Quality of Life Questionnaire) and POMS scores in Ademola 2025 also showed numerical improvements.