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NCT01306422 · ClinicalTrials.gov registry record · NA
Safety, Tolerability, Kinetics and Efficacy Study of Hoodia Gordonii Purified Extract (PYM50717)
A NA study of Overweight and Body Weight, sponsored by Unilever R&D.
- Completed
- Registry status
- NA
- Development phase
- 64
- Enrollment target
- 1
- Study location
NCT01306422 is a NA study of Overweight and Body Weight that has completed, run by Unilever R&D. The registered enrollment target is 64 participants, below the 1,323-participant average among 197 other Overweight trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01306422, a NA study of Overweight and Body Weight, has completed, sponsored by Unilever R&D.
- COMPLETED
- Registry status
- NA
- Development phase
- 64 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this clinical study was to assess the safety, tolerability, efficacy (effects on appetite scores, food intake) and plasma kinetics of Hoodia gordonii purified extract (H.g.PE), when consumed twice-daily for 2 or 15-days.
Conditions Studied
Interventions
- OTHER Hoodia gordonii purified extract (H.g.PE)
- OTHER Placebo yogurt drink
Study Locations (1)
Wisconsin
- Covance CRU - Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2008-03 |
| Est. Completion | 2008-10 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01306422
The ClinicalTrials.gov registry entry for NCT01306422 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,323-participant average among 197 other Overweight trials with a reported enrollment target (95% lower). The listed sponsor is Unilever R&D, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Overweight appearing as the primary indexed condition, and to 2 interventions - of which Hoodia gordonii purified extract (H.g.PE) is the first listed.
NCT01306422 reports 1 study location spanning 1 distinct geographic area - top geographies include Wisconsin.
Frequently Asked Questions
What is clinical trial NCT01306422 about?
NCT01306422 is a clinical study titled "Safety, Tolerability, Kinetics and Efficacy Study of Hoodia Gordonii Purified Extract (PYM50717)". The objective of this clinical study was to assess the safety, tolerability, efficacy (effects on appetite scores, food intake) and plasma kinetics of Hoodia gordonii purified extract (H.g.PE), when consumed twice-daily for 2 or 15-days.
What is the current status of trial NCT01306422?
This trial is currently completed. It is a NA study. The enrollment target is 64 participants. The study started on 2008-03. Estimated completion is 2008-10.
What conditions does trial NCT01306422 study?
This clinical trial studies the following conditions: Overweight, Body Weight, Appetite Depressant.
What interventions are being tested in trial NCT01306422?
The interventions under investigation include: Hoodia gordonii purified extract (H.g.PE) (OTHER), Placebo yogurt drink (OTHER).
Who is sponsoring clinical trial NCT01306422?
This trial is sponsored by Unilever R&D, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01306422 being conducted?
This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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