No phaseRecruiting

Tirzepatide Titration to Reduce Side Effects in Individuals With Obesity (TiTRE)

Sponsor
Dasman Diabetes Institute (Academic or other)
Enrollment
68 planned
Conditions
Obesity
Interventions
Tirzepatide (Per-label titration); Tirzepatide (Flexible titration)
Ages
adults, older adults
Registry
NCT07574723

Full record on ClinicalTrials.gov

From the registry

The goal of this clinical trial is to determine whether a flexible, symptom-guided titration strategy for tirzepatide can help adults with obesity without diabetes stay on treatment longer, while maintaining weight-loss effectiveness. The main questions it aims to answer are: * Does flexible, symptom-guided titration increase time on treatment (delay treatment discontinuation) compared with standard per-label titration over 76 weeks? * Does flexible titration reduce gastrointestinal side effects, such as nausea and vomiting, compared with standard titration? * Does flexible titration achieve weight loss comparable to standard titration? Researchers will compare standard per-label titration with a click-based, symptom-guided titration approach to assess differences in treatment persistence, tolerability, and effectiveness. Participants will: * Be randomly assigned to standard or flexible tirzepatide titration * Use a click-based dosing method that allows small dose increases based on tolerability (flexible group) * Attend study visits over 76 weeks for safety and outcome…

Primary outcomes

  • Time to discontinuation of the treatment regimen

History

  1. Study completion expected

  2. Primary completion expected

  3. Last registry update

  4. Started

  5. Registered