Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite
Not a traditional drug phase: testing Tirzepatide (Per-label titration) for Obesity
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?
This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.
Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
What the registry says happens
If you join, the listed intervention(s) are Tirzepatide (Per-label titration), or Tirzepatide (Flexible titration). The registry lists allocation as randomized. 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.
They plan to enroll about 68 people at Kuwait City. Taking part typically means taking a study drug (or dummy pill) plus check-ins.
Official title (unrewritten)
Tirzepatide Titration to Reduce Side Effects (TiTRE) in Individuals With Obesity
Primary outcome (registry wording): Time to discontinuation of the treatment regimen
Who it is for (from inclusion criteria)
Ages 18 Years to 100 Years
Adults aged 18 years and older
A diagnosis of obesity (body-mass index (BMI) ≥ 27 kg/m2) at screening with self-reported unsuccessful dietary efforts to lose weight
No diagnosis of diabetes mellites
Able to undergo DEXA scan
Who the registry excludes
1\. History of type 1 or type 2 diabetes mellites. 2. Obesity-related:
A self-reported change in body weight \>5 kg (11 lbs) within 90 days before screening irrespective of medical records
Treatment with any medication for the indication of obesity within the past 90 days before screening
Current use, or use within 90 days before screening, of medications with the potential to increase body weight (e.g., systemic glucocorticosteroids, antipsychotics, antidepressants, and antiepileptics) or to reduce body weight (e.g., diuretics)
Uncontrolled thyroid disease, defined as thyroid stimulating hormone \>6.0 mIU/L or \<0.4 mIU/L as measured by the central laboratory at screening
History of major depressive disorder within 2 years before screening
Diagnosis of other severe psychiatric disorder (e.g. schizophrenia, bipolar disorder)
Contact
No central phone on the registry card. Use the official listing to reach a site.
Sites listed on ClinicalTrials.gov
1 listed
Dasman Diabetes Institute — Kuwait City, Kuwait (recruiting)
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The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.
What phase is NCT07574723?
Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.
Can PlainTrials tell me if I qualify for NCT07574723?
No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.