Status:

RECRUITING

The Renal Protective Effects of Remote Ischemic Preconditioning in Patients With Chronic Kidney Disease

Lead Sponsor:

Yuanjun Yang

Conditions:

Chronic Kidney Diseases

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The incidence of Chronic kidney disease (CKD) is showing an upward trend, but the therapeutic effect of treatment is limited. Remote ischemic conditioning (RIC) has the potential to safeguard remote o...

Detailed Description

Chronic kidney disease (CKD) is characterized by progressive and irreversible loss of nephrons. Currently, due to the increasing prevalence of diabetes, hypertension, obesity, and the impact of popula...

Eligibility Criteria

Inclusion

  • CKD Patients with eGFR ≥ 15ml/min/1.73m2
  • Age ≥ 18 years old
  • 24-hour urine protein excretion ≤ 3.5g
  • Subjects who have signed the informed consent form

Exclusion

  • Patients with nephrotic syndrome
  • Patients with acute kidney injury
  • Patients who have undergone renal replacement treatment in the past
  • Patients who may have medication changes during RIC or sham-RIC intervention
  • Patients with a history of diabetes or glycated hemoglobin \> 8%
  • Patients with familial hypercholesterolemia (\>5.5 mmol/L) accompanied by high low-density lipoprotein (\>2.5 mmol/L)
  • Patients with contraindications to RIC, such as vascular injury, soft tissue injury, fracture, infection, or known peripheral vascular disease in both arms
  • Patients with a history of hemostatic disorders, systemic bleeding, or thrombocytopenia
  • Patients with cardiogenic embolism (atrial fibrillation) or other severe arrhythmias (severe bradycardia, third-degree atrioventricular block, or ventricular tachycardia), previous myocardial infarction, or severe heart failure (New York Heart Association Class III and IV)
  • Uncontrolled hypertension (defined as systolic blood pressure ≥ 200 mmHg despite antihypertensive treatment)
  • Patients with respiratory failure, malignant tumors, or other autoimmune diseases
  • Women who are pregnant or breastfeeding at the time of enrollment or any time during the study

Key Trial Info

Start Date :

March 1 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 30 2027

Estimated Enrollment :

114 Patients enrolled

Trial Details

Trial ID

NCT06501222

Start Date

March 1 2024

End Date

March 30 2027

Last Update

August 19 2024

Active Locations (1)

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Page 1 of 1 (1 locations)

1

chinese PLA general hospital

Beijing, Beijing Municipality, China, 100853