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NCT06244147 · ClinicalTrials.gov registry record

Long Term Safety and Efficacy of KSM-66 Ashwagandha in Adults

A clinical trial, sponsored by SF Research Institute.

Completed
Registry status
200
Enrollment target

NCT06244147: Completed study, sponsored by SF Research Institute.

NCT06244147 is a clinical trial that has completed, run by SF Research Institute. The registered enrollment target is 200 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06244147 has completed, sponsored by SF Research Institute.

COMPLETED
Registry status
200 participants
Enrollment target

Study Summary

The primary objective is to evaluate the clinical safety of KSM-66 Ashwagandha (Withania Somnifera) on long-term administration over 12 months. The secondary objectives are to evaluate the laboratory safety of KSM-66 Ashwagandha (Withania Somnifera) on long-term administration over 12 months and to evaluate the efficacy of KSM-66 Ashwagandha (Withania Somnifera) on long-term administration over 12 months.

Primary Outcome

Number and proportion of Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Event (TESAE) due to KSM-66 Ashwagandha (Withania Somnifera) over 12 months period

Interventions

  • DIETARY_SUPPLEMENT KSM-66 Ashwagandha Root Extract

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2024-02-15
Est. Completion 2025-10-15
SF Research Institute

16 total trials

What the finished NCT06244147 record still lists

NCT06244147 is an observational study that tracks outcomes without assigning an intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 1 intervention - of which KSM-66 Ashwagandha Root Extract is the first listed.

NCT06244147 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06244147 about?

NCT06244147 is a clinical study titled "Long Term Safety and Efficacy of KSM-66 Ashwagandha in Adults". The primary objective is to evaluate the clinical safety of KSM-66 Ashwagandha (Withania Somnifera) on long-term administration over 12 months. The secondary objectives are to evaluate the laboratory safety of KSM-66 Ashwagandha (Withania Somnifera) on long-term administration over 12 months and to ...

What is the current status of trial NCT06244147?

This trial is currently completed. The enrollment target is 200 participants. The study started on 2024-02-15. Estimated completion is 2025-10-15.

What interventions are being tested in trial NCT06244147?

The interventions under investigation include: KSM-66 Ashwagandha Root Extract (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT06244147?

This trial is sponsored by SF Research Institute, which has 16 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT06244147, the US trial registry maintained by the National Library of Medicine. NCT06244147 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.