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Enrolling By InvitationNCT06959784

Assessing Incretin Therapy for Cardiovascular Risk Reduction and Diabetes Remission( ITCRDR Study)

Evidence Based Evaluation of Incretin Drugs in Reducing the Risk of Cardiovascular and Cerebrovascular Events and Promoting the Remission of Diabetes

Status
Enrolling By Invitation
Phase
Phase 4
Study type
Interventional
Enrollment
142 (estimated)
Sponsor
China-Japan Friendship Hospital · Academic / Other
Sex
All
Age
30 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This study used the diabetes prevention and follow-up research queue in Daqing and the public database of UKbiobank to evaluate the risk factors of cardiovascular and cerebrovascular events in diabetes patients, and built the first risk prediction model of cardiovascular and cerebrovascular events in diabetes patients based on the Chinese population follow-up queue and externally verified, so as to identify high-risk groups and guide the early prevention of cardiovascular and cerebrovascular diseases in diabetes patients. To evaluate the effect of incretin drugs on reducing the risk of cardiovascular and cerebrovascular events, and the impact on the remission rate of diabetes in people with initial diabetes, a randomized, multicenter, controlled clinical study was conducted. The long-term follow-up of 2 years was conducted to evaluate whether the cardiovascular and cerebrovascular risks of those who stopped drug treatment after remission of diabetes compared with those who continued drug treatment were reduced, as well as the long-term impact of incretin on cardiovascular and cerebrovascular risks and the role of long-term mitigation of diabetes.

Conditions

Interventions

TypeNameDescription
DRUGsemaglutideThe semaglutide intervention group received semaglutide (0.25 mg qw initially, increased to 0.5 mg qw after four weeks) for 24 weeks (6 months).
DRUGMetforminThe metformin control group was treated with metformin (gradually increasing to 1g bid) for 24 weeks (6 months)

Timeline

Start date
2024-01-01
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2025-05-07
Last updated
2025-05-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06959784. Inclusion in this directory is not an endorsement.