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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06059287
Other study ID # IIT-2023-0180
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2023
Est. completion date December 31, 2025

Study information

Verified date September 2023
Source RenJi Hospital
Contact Rong Huang
Phone 68-021-68383424
Email renjihuangrong@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective, randomized, open-label, active drug controlled clinical trial that aims to compare the effects of henagliflozin or metformin on myocardial tissue level characteristics in type 2 diabetes patients with obesity. Eligible subjects with type 2 diabetes before randomisation and fulfilling all of the inclusion criteria and none of the exclusion criteria will be randomised in a 1:1 ratio to henagliflozin 10 mg once a day or metformin 1000 mg twice a day and treated for 24 weeks. The study includes five visits.


Description:

MRI scanning will be assessed at baseline and at the end of the treatment period in order to to assess the cardiac morphology, cardiac function, and myocardial tissue characteristics. The cardiac MRI examination will be performed in accordance with a pre-defined MRI protocol. Images from all sites will be analyzed centrally at the core-lab using a dedicated software package and certified analysts.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 64
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Individuals with type 2 diabetes newly diagnosed based on the WHO (1999) criteria; - Hemoglobin A1c levels >=7.0% and <=8.0%; - Females or males =18 years up to 75 years of age. Exclusion Criteria: - Females or males <18 years. - Clinical diagnosis of type 1 diabetes and other types of diabetes. - Blood pressure at screening that would require a change in blood pressure treatment over the study period. - History of stroke or other clinically significant cerebrovascular disease. - Any of the following cardiovascular diseases: 1. Atrial fibrillation, or other unstable or severe arrhythmia affecting heart function 2. Unstable heart failure or any heart failure with NYHA class III and IV 3. Significant valvular disease 4. Significant peripheral artery disease - Active malignancy requiring treatment at the time of visit 0. - Patients with severe hepatic impairment. - Unstable or rapidly progressing renal disease. - Ongoing treatment with loop diuretics. - Estimated Glomerular Filtration Rate (eGFR) <45 mL/min/1.73 m2. - Women who has a positive pregnancy test at enrolment or randomization, or are breastfeeding.

Study Design


Intervention

Drug:
Henagliflozin
Henagliflozin 10mg qd po
Metformin
Metformin 1000mg bid po

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
RenJi Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Extra-cellular volume fraction To compare the effects of henagliflozin and metformin on extra-cellular volume fraction baseline and week 24
Secondary Mean Change in HbA1c Levels To compare the effects of henagliflozin and metformin on HbA1c Levels baseline and week 24
Secondary Mean change in body mass index To compare the effects of henagliflozin and metformin on body mass index baseline and week 24
Secondary Mean change in blood pressure To compare the effects of henagliflozin and metformin on blood pressure baseline and week 24
Secondary Mean change in level of Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) To compare the effects of henagliflozin and metformin on level of Homeostatic Model Assessment of Insulin Resistance baseline and week 24
Secondary Native T2 mapping To compare the effects of henagliflozin and metformin on native T2 mapping baseline and week 24
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