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NCT05507008 · ClinicalTrials.gov registry record · NA
Ketone Supplementation in Eating Disorders
A NA study of Anorexia Nervosa and Bulimia Nervosa, sponsored by University of California, San Diego.
- Active
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 1
- Study location
NCT05507008 is a NA study of Anorexia Nervosa and Bulimia Nervosa that is active but no longer recruiting, run by University of California, San Diego. The registered enrollment target is 40 participants, below the 949-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05507008, a NA study of Anorexia Nervosa and Bulimia Nervosa, is active but no longer recruiting, sponsored by University of California, San Diego.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will investigate the effects of ketone supplementation on eating behavior including drive to binge eat or restrict, mood and anxiety in individuals with anorexia or bulimia nervosa. In addition, the investigators will contrast the effects of active ketone supplementation versus placebo on electroencephalogram (EEG) measurement. All subjects enrolled in the study will undergo EEG on two consecutive days at the beginning of the study, after active ketone supplementation or placebo drink, matched in taste to the ketone drink. Days will be randomized. Thereafter, all subjects will take the ketone supplementation drink for two weeks, twice daily.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Kenetik Ketone Drink
Study Locations (1)
California
- University of California San Diego - San Diego
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2022-10-13 |
| Est. Completion | 2026-12-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05507008
The ClinicalTrials.gov registry entry for NCT05507008 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 949-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (96% lower). The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Anorexia Nervosa appearing as the primary indexed condition, and to 1 intervention - of which Kenetik Ketone Drink is the first listed.
NCT05507008 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT05507008 about?
NCT05507008 is a clinical study titled "Ketone Supplementation in Eating Disorders". This study will investigate the effects of ketone supplementation on eating behavior including drive to binge eat or restrict, mood and anxiety in individuals with anorexia or bulimia nervosa. In addition, the investigators will contrast the effects of active ketone supplementation versus placebo on...
What is the current status of trial NCT05507008?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2022-10-13. Estimated completion is 2026-12-30.
What conditions does trial NCT05507008 study?
This clinical trial studies the following conditions: Anorexia Nervosa, Bulimia Nervosa, Atypical Anorexia Nervosa, Atypical Bulimia Nervosa.
What interventions are being tested in trial NCT05507008?
The interventions under investigation include: Kenetik Ketone Drink (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT05507008?
This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05507008 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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