Efficacy and Safety of Bariatric Surgery, Semaglutide Once Weekly, and Tirzepatide Once Weekly in Patients With Obesity

Status: Recruiting
Location: See location...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The recent introduction of the new generation of anti-obesity medications (AOMs) will change the future of obesity treatment. These highly effective medications, such as high-dose semaglutide and tirzepatide, are hormone analogues that augment the incretin function and exert multiple physiological effects by activating glucagon-like peptide-1 (GLP-1) and/or glucose-dependent insulinotropic polypeptide (GIP) distributed in various organs. These medications provide an average of 15-22% weight reduction in one-year trials, which had not been seen in the past with medical therapy. While the literature suggests that bariatric surgery is superior to these new highly effective medications, there is no head-to-head comparison between the most common bariatric operations (Roux-en-Y gastric bypass \[RYGB\] and sleeve gastrectomy \[SG\]) with semaglutide (once weekly) and tirzepatide (once weekly). The goal of this Randomized Clinical Trial (RCT) is to compare these effective therapies in patients with severe obesity to provide the best evidence to inform clinical decisions in treating patients with obesity.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

‣ Entry into the study would require that the patient:

• Is a candidate for general anesthesia

• Is eligible for bariatric surgery (RYGB or SG) based on ASMBS/IFSO 2022 guidelines

• Is ≥18 and ≤70 years old (both inclusive)

• has a BMI ≥35 and ≤65 kg/m2 (both inclusive)

• Patients with and without T2DM are eligible for the study. Patients with T2DM should have been on a stable dose of anti-diabetic medication (including insulin but not semaglutide or tirzepatide) for at least 3 months prior to entry, with HbA1c ≤12%.

• No weight loss \> 20 lbs. in 3 months before screening (self-reported)

• Has the ability and willingness to participate in the study, provide informed consent, and agree to any of the arms involved in the study.

• Is able to understand the options and to comply with the requirements of each arm.

• Has a negative urine pregnancy test at randomization visit for women of childbearing potential.

⁃ Women of childbearing age must agree to use reliable method of contraception for 2 years.

Locations
United States
Ohio
The Cleveland Clinic
RECRUITING
Cleveland
Contact Information
Primary
Chytaine Hall
hallc1@ccf.org
(216) 445-3983
Backup
Roham Foroumadi, MD
foroumr@ccf.org
(216) 445-0045
Time Frame
Start Date: 2025-01-29
Estimated Completion Date: 2027-12-01
Participants
Target number of participants: 125
Treatments
Active_comparator: Bariatric Surgery
Roux-en-Y Gastric Bypass (RYGB) and Sleeve Gastrectomy (SG)
Active_comparator: Semaglutide
Semaglutide, which is an incretin-based medication that has been approved for the treatment of obesity, will be used for this arm.
Active_comparator: Tirzepatide
Tirzepatide, which is an incretin-based medication that has been approved for the treatment of obesity, will be used for this arm.
Related Therapeutic Areas
Sponsors
Collaborators: Ethicon, Inc.
Leads: Ali Aminian

This content was sourced from clinicaltrials.gov