Actively Recruiting

Phase 4
Age: 18Years - 70Years
All Genders
NCT06461377

The Ameliorative Effects of GLP-1RA on Diabetic Cardiac Autonomatic Neuropathy

Led by The First Affiliated Hospital with Nanjing Medical University · Updated on 2024-06-21

50

Participants Needed

1

Research Sites

185 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Diabetic cardiac autonomic neuropathy (DCAN) is a common chronic complication that reduces survival in patients with diabetes. Epidemiological surveys have shown that the prevalence of DCAN is 25-75% in people with type 2 diabetes. The onset of DCAN is insidious and easy to be ignored in the early stage. With the progression of the disease, the following clinical symptoms gradually appear, including reduced heart rate variability, exercise intolerance, resting tachycardia, orthostatic hypotension, painless myocardial infarction and even sudden death, which seriously endanger the life and health of type 2 diabetes patients. Existing literature has shown that glucagon-like peptide-1 receptor agonist (GLP-1RA) can improve diabetic peripheral neuropathy and diabetic cognitive dysfunction, but there are few studies on improving diabetic autonomic neuropathy. Insulin resistance is an important risk factor for DCAN. Patients with type 2 diabetes are characterized by insulin resistance, and GLP-1RA is recognized as a drug to improve insulin resistance and control blood sugar in patients with diabetes. In this study, GLP-1RA was used to intervene patients with type 2 diabetes, and the changes in blood sugar control and insulin resistance status of patients were followed up. Special attention was paid to the improvement of autonomic neuropathy in diabetic patients.

CONDITIONS

Official Title

The Ameliorative Effects of GLP-1RA on Diabetic Cardiac Autonomatic Neuropathy

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-70 years
  • Patients diagnosed with type 2 diabetes mellitus
  • Signed informed consent form
  • Being overweight or obese
Not Eligible

You will not qualify if you...

  • Under 18 years old
  • Pregnant or lactating women
  • Acute or chronic pancreatitis
  • Recent acute complications of diabetes
  • Arrhythmia or taking drugs that affect heart rate
  • Thyroid disease
  • Severe organ dysfunction
  • Refusal to provide informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

the First Affiliated Hospital of Nanjing Medical University

Nanjing, Jiangsu, China, 210029

Actively Recruiting

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Research Team

J

jianbo Li, MD/PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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