Skip to main content
OpenTrials
Completed

NCT Number: NCT07513259

Pre-Diagnosis GLP-1 Receptor Agonist Use and Post-Cancer Mortality in Adults With Obesity and Type 2 Diabetes

This study will examine whether the type of diabetes treatment used before cancer diagnosis is associated with survival and serious complications after obesity-associated cancer in adults with obesity and type 2 diabetes. The study focuses on glucagon-like peptide-1 receptor agonists (GLP-1 RA) and compares them with other commonly used glucose-lowering therapies, including SGLT2 inhibitors, DPP-4 inhibitors, sulfonylureas, metformin, and usual care. Using de-identified electronic health record data from the TriNetX US Collaborative Network, the study will assess whether patients who used GLP-1 RA before cancer diagnosis have different risks of death, hospitalization, sepsis, and other major outcomes after cancer diagnosis. This is an observational study designed to evaluate associations in routine clinical care and not to prove a treatment effect.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18 years or older
  • BMI ≥27 kg/m2, or diagnosis codes consistent with obesity
  • Type 2 diabetes mellitus
  • Initiation of a glucose-lowering medication before obesity-associated cancer diagnosis
  • Incident obesity-associated cancer diagnosed after medication initiation
  • No dispensing of the study drug class during the 6-month washout period before the first qualifying prescription

Exclusion criteria

  • Type 1 diabetes mellitus, Other specified diabetes types that are not type 2 diabetes
  • Human immunodeficiency virus infection
  • End-stage renal disease
  • Prior bariatric surgery
  • Prior organ transplantation
  • Transplant-related complications
  • Any use of tirzepatide before cohort entry

Treatment and study plan

Primary outcomes

  1. All-Cause Mortality

    Time frame: Up to 36 months after obesity-associated cancer diagnosis

    Time to all-cause mortality after obesity-associated cancer diagnosis among adults with obesity and type 2 diabetes according to pre-diagnosis glucose-lowering treatment strategy.

Secondary outcomes

  1. All-Cause Inpatient Hospitalization

    Time frame: Up to 36 months after obesity-associated cancer diagnosis

    Time to first all-cause inpatient hospitalization after obesity-associated cancer diagnosis.

  2. Sepsis

    Time frame: Up to 36 months after obesity-associated cancer diagnosis

    Time to first sepsis event after obesity-associated cancer diagnosis.

  3. Pulmonary Embolism

    Time frame: Up to 36 months after obesity-associated cancer diagnosis

    Time to first pulmonary embolism event after obesity-associated cancer diagnosis.

  4. Pericardial Effusion

    Time frame: Up to 36 months after obesity-associated cancer diagnosis

    Time to first pericardial effusion event after obesity-associated cancer diagnosis.

Sponsors and collaborators

Lead sponsor

Chung Shan Medical University

Other

Collaborators

  • National Science and Technology Council, Taiwan

Registry information

Official study title

Pre-Diagnosis GLP-1 Receptor Agonist Use and Post-Cancer Mortality in Adults With Obesity and Type 2 Diabetes: A Target Trial Emulation

Important dates

Study start
2018
Primary completion
2025
Study completion
2025
First posted
Apr 7, 2026
Registry last updated
Apr 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.