Study details
Enrolling now
Efficacy and Safety of Ashwagandha Root Extract
SF Research Institute, Inc.
NCT IDNCT06714942ClinicalTrials.gov data as of Apr 2026
Target enrollment
51
Study length
about 3 months
Ages
18–65
Locations
1 site in CA
About this study
This trial is testing a proprietary blend of ashwagandha root extract to see if it helps with stress and anxiety in adults. Participants will be randomly assigned to take either the ashwagandha blend, KSM-66 ashwagandha extract, or a placebo twice daily for 8 weeks. The goal is to compare the effectiveness and safety of these treatments.
Based on ClinicalTrials.gov records.
What participants do
- 1.KSM-66 Ashwagandha root extract
- 2.Placebo
- 3.Proprietary Blend of Ashwagandha
Participation effort
Estimated from trial records. Details can vary by site.
Time + visits
Low14%
Logistics
Moderate50%
Logistics difficulty varies by site location and availability.
Trial highlights
Treatment details
Auto-extracted from trial records to preview treatments and outcomes.
Endpoints
Secondary: Hamilton Anxiety Rating Scale (HAM-A), Perceived Stress Scale Score (PSS)
Body systems
Psychiatry / Mental Health