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NCT07441109

Shatavari Root Extract for Perimenopausal Symptoms

Not yet recruiting NA Last updated 3 March 2026
What this trial tests

NA trial testing Shatavari (Asparagus racemosus) Root Extract in Perimenopause in 60 participants. Not yet recruiting.

Timeline
11 March 2026
Primary endpoint
15 June 2026
29 June 2026

Quick facts

Lead sponsorSF Research Institute, Inc.
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment60
Start date11 March 2026
Primary completion15 June 2026
Estimated completion29 June 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

SF Research Institute, Inc.

Who can join

Adults 40 to 45, female only, with Perimenopause or Women Health. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This randomized, double-blind, placebo-controlled clinical study evaluates the efficacy and safety of a standardized Shatavari (Asparagus racemosus) root extract in women experiencing perimenopausal symptoms. Participants will receive either Shatavari root extract or a matched placebo for 12 weeks. Efficacy will be assessed using validated menopause-specific symptom, quality-of-life, stress, mood, and sleep questionnaires, along with physiological stress markers. Safety will be evaluated through laboratory assessments and adverse event monitoring.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Shatavari (Asparagus racemosus) Root Extract

Trials testing the same drug.

Other recruiting trials for Perimenopause

Currently open trials in the same condition.

Other SF Research Institute, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07441109.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing