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Effectiveness and Safety of Semaglutide and Tirzepatide in the Treatment of Type 2 Diabetes Mellitus

Effectiveness and Safety of Semaglutide and Tirzepatide as Add-on therapy in Type 2 Diabetes Mellitus patients: An Ambispective cohort study in real-world setting - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/113158
Enrollment
66
Registered
2026-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E11- Type 2 diabetes mellitus

Interventions

Intervention1: Nil: Nil

Sponsors

Dr Parv Mathur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age greater than or equal to 18 years Males and females T2DM patients starting semaglutide or tirzepatide as add on therapy for the first time at the time of screening Body Mass Index greater than or equal to 23 Kg per m2 Patients who had previously been on antidiabetic drugs for at least 6 months Willing and able to undergo treatment and follow-up as required by the protocol.

Exclusion criteria

Exclusion criteria: Any known significant gastric emptying and severe gastrointestinal diseases at screening Female who is pregnant or intends to become pregnant during the study period, or is lactating at the time of screening

Design outcomes

Primary

MeasureTime frame
To evaluate the effectiveness of semaglutide and tirzepatide as add-on therapy in HbA1c reduction and reduction in body weight To assess the safety of semaglutide and tirzepatideTimepoint: Assessment at baseline, 1 month, 3 months and 6 months

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Anuradha HV

MS Ramaiah Medical College, Bengaluru

anuradhahv.rmc@msruas.ac.in9448847946

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026