Comprehensive Clinical Evaluation Study of GLP-1RA

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The objective of this project is to identify the most efficacious glucagon-like peptide-1 receptor agonists (GLP-1RAs) for the treatment of adult patients with type 2 diabetes mellitus (T2DM). In accordance with the index system and evaluation rules set forth in the Management Guidelines for Comprehensive Clinical Evaluation of Drugs, the effects of GLP-1RAs drugs in real-world settings are tracked, summarised, and analysed across six dimensions: safety, effectiveness, economy, innovation, appropriateness, and accessibility. This is done with the objective of ensuring that these drugs are fully utilised in accordance with their potential benefits. The objective is to ascertain the role of medical institutions as the principal entity responsible for the comprehensive evaluation of the clinical application of drugs and to provide data that will reduce the risk of using GLP-1RAs drugs. Moreover, the objective is to ascertain the advantages of their clinical application and to guarantee the safe and rational use of drugs for patients with type 2 diabetes mellitus. The objective of this study is to facilitate the fulfilment of medical institutions' role as the primary entity responsible for the comprehensive evaluation of the clinical application of medicines. Furthermore, the study will provide data that can be used to reduce the risk of using GLP-1RAs drugs, explore the advantages of their clinical application, and guarantee the safe and rational use of medicines for patients with type 2 diabetes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosed with type 2 diabetes;

• no study drug has been used in the last three months;

• Existing hypoglycemic programs include investigational drugs;

• Age ≥18 years old;

• The patient's demographic data, disease history, course records, laboratory test indicators, drug use and other information were complete;

• Sign informed consent.

Locations
Other Locations
China
Yan Li
RECRUITING
Jinan
Contact Information
Primary
Dong Zhonghua The First Affiliated Hospital of Shandong First Medical Univer, master
dzh941213@163.com
+8618253161252
Time Frame
Start Date: 2024-07-01
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 492
Treatments
liraglutide
Dulagoside
Polyethylene glycol losenatide
Semaglutide
Related Therapeutic Areas
Sponsors
Leads: LI YAN

This content was sourced from clinicaltrials.gov