Comparative Study of Different Weekly GLP-1 Receptor Agonists Among Diabetic and Non-Diabetic Patients: Clinical Trial
- Sponsor
- Zagazig University
- Study ID
- NCT07820111
- Phase
- PHASE3
- Status
- Completed
Conditions
- Obese Diabetics
- Obese Non Diabetic
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- Dulaglutide 1.5 MG/ML — DRUGonce weekly dulaglutide injection
- Semaglutide 2 mg/1.5 ml (1.34 mg/ml), prefilled pen-injector for subcutaneous injection solution — DRUGonce weekly
- Tirzepatide is administered as part of routine clinical care for obesity management, according to standard prescribing practices. Dosing and treatment duration are determined by the treating physician — DRUGonce weekly tirzeptide 7.5 and 15 mg
- Dulaglutide 0.75mg subcutaneous injection — DRUGonce weekly
- Semaglutide 1.0 mg — DRUGonce weekly
- Tirzepatide (Flexible titration) — DRUGonce weekly
Study Details
titel : Comparative Study of Different Weekly GLP-1 Receptor Agonists Among Diabetic and Non-Diabetic Patients: Clinical Trial Abstract : Background: This study that highlights the different effects of most used three GLP-RA Dulaglutide, Semaglutide, Tirazepetide among diabetic and non -diabetic participant as the well-known fact that they don't have only weight recuing effect but also many different effects on metabolic process including insulin sensitivity, lipid profile and NASH. Materials and Methods: This is a randomized controlled study involving a total of 159 participants, divided into 75 non-diabetic and 84 diabetic obese individuals. Participants were assigned to three drug groups, each receiving a once-weekly dose of Dulaglutide, Semaglutide, or Tirzepatide for a period of 24 weeks. Each drug group consisted of 53 individuals, subdivided into 25 non-diabetic and 28 diabetic participants. Measurements were taken at three time points: pretreatment, 3 months post-treatment, and 6 months post-treatment. Each participant underwent a complete physical exam, and data was collected on weight, BMI, age, and sex and Laboratory tests. , also repeated measurements were taken at 3 and 6 months post-treatment. on metabolic processes, weight reduction, and insulin sensitivity, particularly in diabetic individuals, as well as effects on lipid profiles and liver enzymes, weight reduction, BMI, HbA1c, TYG-index, triglycerides, and HDL-C levels. total cholesterol (Tc) and liver enzymes. Data were collected, and statistical analyses were conducted afterward.
Key Dates
- First listed
- Sep 15, 2026
- Start date
- Oct 18, 2025
- Status verified
- Sep 2026
- Primary completion
- Mar 17, 2026
- Completion
- Mar 17, 2026
Study Design
- Enrollment
- 159 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: obese , non diabetic ,recieve dulaglutideGLP1-RA
- Active Comparator: obese , non diabetic ,receive SEMAGLUTIDEGLP1-RA
- Active Comparator: obese , non diabetic ,receive TIRAZEPETIDEGLP1-RA
- Active Comparator: obese , diabetic ,recieve dulaglutideGLP1-RA
- Active Comparator: obese , diabetic ,receive SEMAGLUTIDEGLP1-RA
- Active Comparator: obese , diabetic ,receive TIRAZEPETIDEGLP1-RA
Primary Outcome Measure
change in body weight at 3 and 6 months [ Time Frame: 6-MONTH STUDY PERIOD ]
Related coverage on Hipa.ai
- Dulaglutide Phase 3 Trial Comparing Weekly GLP-1 Drugs CompletedDulaglutide · Mar 17, 2026 · ClinicalTrials.gov