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Study details
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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.KSM-66 Ashwagandha root extract
  • 2.Placebo
  • 3.Proprietary Blend of Ashwagandha

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Secondary: Hamilton Anxiety Rating Scale (HAM-A), Perceived Stress Scale Score (PSS)

Body systems

Psychiatry / Mental Health