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Preventing Weight Regain Post-Semaglutide Treatment With Active Fiber Supplement (Soloways) - Trial NCT06221696

Access comprehensive clinical trial information for NCT06221696 through Pure Global AI's free database. This phase not specified trial is sponsored by S.LAB (SOLOWAYS) and is currently Completed. The study focuses on Overweight and Obesity. Target enrollment is 160 participants.

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NCT06221696
Completed
dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT06221696
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Preventing Weight Regain Post-Semaglutide Treatment With Active Fiber Supplement (Soloways)
Preventing Weight Regain Post-Semaglutide Treatment With Active Fiber Supplement (Soloways): A Randomized, Placebo-Controlled, Double-Blind Clinical Trial

Study Focus

Overweight and Obesity

Active Fiber Supplement Group

Interventional

dietary supplement

Sponsor & Location

S.LAB (SOLOWAYS)

Novosibirsk, Russian Federation

Timeline & Enrollment

N/A

Jun 12, 2023

Dec 01, 2023

160 participants

Primary Outcome

Percentage of weight regain from baseline

Summary

This randomized, double-blind, placebo-controlled trial titled Preventing Weight Regain
 Post-Semaglutide Treatment with Active Fiber Supplement (Soloways) evaluated the efficacy of
 an active fiber supplement in preventing weight regain post-Semaglutide treatment.
 Participants were adults aged 18-65, with a history of obesity or overweight, and had
 completed a Semaglutide course. The study involved 160 participants, equally divided into two
 groups: one receiving the active fiber supplement (glucomannan, inulin, and psyllium) and the
 other a placebo, both taken 30 minutes before each main meal for 180 days. Co-primary
 endpoints were the percentage of weight regain from baseline to day 180 and metabolic health
 markers (blood glucose levels, HbA1c, lipid profile, blood pressure). Secondary endpoints
 included changes in BMI, body composition, and appetite assessment using VAS ratings and the
 Control of Eating Questionnaire (CoEQ). Participants also adhered to a reduced-calorie diet
 and increased physical activity, with all standard assays performed in a central laboratory.
 The study's objective was to determine the supplement's effectiveness in enhancing satiety,
 improving digestive health, and thus better managing weight compared to a placebo

ICD-10 Classifications

Obesity
Other obesity
Obesity due to excess calories
Obesity, unspecified
Obesity and other hyperalimentation

Data Source

ClinicalTrials.gov

NCT06221696

Non-Device Trial