The Effect of Related Blood Markers on Diabetic Peripheral Neuropathy

W

Wenzhou Medical University

Status

Enrolling

Conditions

Diabetic Peripheral Neuropathy

Study type

Observational

Funder types

Other

Identifiers

NCT06041412
DPN

Details and patient eligibility

About

The goal of this observational study is to explore the relationship between related blood indicators and diabetic peripheral neuropathy(DPN).

Full description

This is a multicenter study(approximately four) with over 1000 subjects.Clinical data were collected by consulting the patient's electronic history. The data included demographic information, blood biochemical markers and electromyography. All participants provided their written informed consent to participate in this study.The study protocol was approved by the Ethics Committee of the First Affiliated Hospital of Wenzhou Medical University(KY-2022-R009).

Enrollment

1,400 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

patients who had undergone nerve conduction examination by electromyography.

Exclusion criteria

  • pregnancy and lactation; chronic liver disease, kidney disease, arrhythmias, malignant diseases, severe respiratory diseases, heart failure, and acute infections;
  • patients with alcohol abuse; history of Autoimmune liver disease, liver disease or abnormal liver function at baseline;
  • parathyroid diseases (including hyperthyroidism and hypothyroidism);
  • pancreatitis, pancreatectomy or any transplant;
  • patients with malignancy and any serious concomitant disease limit the existence of life expectancy

Trial design

1,400 participants in 3 patient groups

DPN group
Description:
Patients with type 2 diabetic peripheral neuropathy were categorized into the DPN group
Diabetic group
Description:
patients with type 2 diabetes mellitus but not with DPN were distributed into the Diabetic group.
control group
Description:
The other individuals without type 2 diabetes mellitus were selected as the control group

Trial contacts and locations

0

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Central trial contact

Binbin Deng

Data sourced from clinicaltrials.gov

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