Registry update — unassessed
Effectiveness of Alternative Therapies in Maintaining Weight Loss Achieved by GLP-1 Medications Post-Cessation: A Randomized, Controlled Trial
Trial registry update: RECRUITING. No results reported in the supplied registry record.
RCTNotable significance
What this changes
The finding has not established an approved change to our evidence assessment.
Source date: Jul 30, 2025 · Discovered: Sep 15, 2026 · Assessed: — · Historical research backfill
What it does not prove
- No outcomes are reported, so this study proves nothing—it describes a planned investigation only
- The study protocol does not indicate whether enrollment was completed, participants were followed to endpoint, or any data were collected
- Even when completed, results from this single trial would require replication to establish whether metformin combinations are effective for weight maintenance after GLP-1 cessation
Extracted from supplied source material; model confidence is not a measured probability of correctness.
Study details
- Design
- Rct
- Sample size
- —
- Duration
- 6 months
- Population
- Patients weaning off GLP-1 medications who have achieved weight loss
- Primary outcome
- Percentage of weight regain six months after cessation of GLP-1 therapy
- Effect size
- —
- Significance
- Not reported
- Journal
- AgelessRx
- Published
- Jul 30, 2025
Sources
Primary source
- AgelessRx ↗Clinical trial
Recorded source passages
Abstract or registry material supplied for assessment; source version 1. This is not a claim of full-text review.
The goal of this randomized, controlled trial is to evaluate the effectiveness of alternative therapies (metformin alone, with rapamycin, and with low-dose naltrexone) in maintaining weight loss in patients weaning off GLP-1 medications.
Researchers will compare the four groups: 1) control, 2) metformin, 3) metformin + rapamycin, and 4) metformin + low-dose naltrexone, to assess changes in the percentage of weight regain, metabolic indicators (e.g., HbA1c, lipid profile), and quality of life PROs, six months after cessation of GLP-1 therapy.
Participants will: Administer the assigned intervention following a dosing and administration protocol provided by the study and medical team.
Source versions
Assessment history
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