Clinical Trials Directory

Trials / Completed

CompletedNCT06215196

Effectiveness and Safety of Semaglutide Combined With Dietary Fiber (Soloways) in Adults With Overweight or Obesity

Effectiveness and Safety of Semaglutide Combined With Dietary Fiber (Soloways) in Adults With Overweight or Obesity: A Randomized, Placebo-Controlled, Double-Blind Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
81 (actual)
Sponsor
S.LAB (SOLOWAYS) · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This clinical trial investigated the combined effects of Semaglutide and a fiber supplement (glucomannan, inulin, psyllium) on weight loss in adults with overweight or obesity. Participants, aged 18-65 with a BMI ≥30 or ≥27 with comorbidities, were randomized into two groups: one receiving Semaglutide with active fiber supplements and the other with Semaglutide and placebo, over a 180-day period. Key endpoints included percentage change in body weight, BMI, body composition, safety, and appetite control, with a focus on evaluating the additive effects of dietary fibers in enhancing Semaglutide's efficacy.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTFiber Supplement GroupSemaglutide (2.4 mg weekly). Three daily packets of active fiber supplement (each containing 1g of glucomannan, 1g of inulin, and 3g of psyllium), taken 30 minutes before each main meal. The supplement is provided by S.Lab (Soloways), LLC.
OTHERplaceboSemaglutide (2.4 mg weekly). Three daily packets of placebo powder, taken 30 minutes before each main meal.

Timeline

Start date
2023-04-14
Primary completion
2023-06-28
Completion
2023-08-20
First posted
2024-01-22
Last updated
2024-01-23

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT06215196. Inclusion in this directory is not an endorsement.