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NCT05863507 · ClinicalTrials.gov registry record · NA
The Influence of Daily Grapes Intake on Sarcopenia in Postmenopausal Women
A NA study of Sarcopenia, sponsored by University of California, Davis.
- Completed
- Registry status
- NA
- Development phase
- 15
- Enrollment target
- 1
- Study location
NCT05863507 is a NA study of Sarcopenia that has completed, run by University of California, Davis. The registered enrollment target is 15 participants, below the 80-participant average among 41 other Sarcopenia trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05863507, a NA study of Sarcopenia, has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
- 1
- Study location
Study Summary
Sarcopenia, characterized by loss of muscle mass and function, is a prevalent disorder in elderly individuals or individuals with chronic diseases. Given the above, there is an ongoing intensive search for novel therapies, including dietary ones, that can attenuate the loss of muscle mass and strength in the elderly. A proposed mechanism by which skeletal muscles might mediate their protective effect against sarcopenia is by secreting myokines as irisin. Phenolic compounds presents in grape have shown to be able to induce irisin secretion in muscle from rats supplemented with a grape pomace extract. The Ian of this study is to evaluate this mechanism in humans.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Grape powder supplementation
Study Locations (1)
California
- Nutrition Department, Ragle Facility University of California, Davis - Davis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2023-04-01 |
| Est. Completion | 2024-07-14 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05863507
The ClinicalTrials.gov registry entry for NCT05863507 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 80-participant average among 41 other Sarcopenia trials with a reported enrollment target (81% lower). The listed sponsor is University of California, Davis, which has 657 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Sarcopenia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT05863507 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT05863507 about?
NCT05863507 is a clinical study titled "The Influence of Daily Grapes Intake on Sarcopenia in Postmenopausal Women". Sarcopenia, characterized by loss of muscle mass and function, is a prevalent disorder in elderly individuals or individuals with chronic diseases. Given the above, there is an ongoing intensive search for novel therapies, including dietary ones, that can attenuate the loss of muscle mass and streng...
What is the current status of trial NCT05863507?
This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2023-04-01. Estimated completion is 2024-07-14.
What conditions does trial NCT05863507 study?
This clinical trial studies the following conditions: Sarcopenia.
What interventions are being tested in trial NCT05863507?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Grape powder supplementation (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT05863507?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05863507 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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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.