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Clinical Trial Summary

The effect of polyethylene glycol Losenatide on body fat, insulin resistance, weight, blood sugar, blood lipid, stomach volume and other factors in patients with type 2 diabetes through 12 week follow-up, and explore the factors affecting the efficacy, so as to provide more evidence-based medical basis for drug treatment and benefit patients.


Clinical Trial Description

The aim of the study is to investigate the factors influencing the efficacy of 12 week treatment with polyethylene glycol Losenatide in type 2 diabetes patients on the basis of diet and exercise. With the 12 week decrease of HbA1c<0.4% from the baseline as the cut-off value, the patients were divided into HbA1c decrease<0.4% group and HbA1c decrease ≥ 0.4% group. The clinical characteristics, laboratory indicators, blood glucose fluctuation of subgroups and gene spectrum differences between the groups were analyzed to provide reference for clinical accurate drug use. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05611684
Study type Interventional
Source Nanjing First Hospital, Nanjing Medical University
Contact Jianhua Ma, Doctor
Phone +8618951670116
Email majianhua196503@126.com
Status Recruiting
Phase Phase 4
Start date June 1, 2022
Completion date December 31, 2025

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