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NCT06501222Recruiting

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

The Renal Protective Effects of Remote Ischemic Preconditioning in Patients With Chronic Kidney Disease: Randomized, Parallel-controlled, proof-of Concept Trial

Source: ClinicalTrials.gov · Last updated 19 Aug 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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 organs via the repeated application of brief ischemic stimuli. the aim of our study is to investigate whether RIC can protect the renal function in patients with CKD.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
114 (estimated)
First submitted
16 Jun 2024
Start date
1 Mar 2024
Primary completion date
30 Mar 2026
Lead sponsor
Yuanjun Yang
NCT number
NCT06501222

What you commit to

  • Study type: Interventional
  • Planned participants: 114
  • From 1 Mar 2024 to the primary completion date, 30 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who may have medication changes during RIC or sham-RIC intervention
  • 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)

Other illness

  • Patients with nephrotic syndrome
  • 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
  • Uncontrolled hypertension (defined as systolic blood pressure ≥ 200 mmHg despite antihypertensive treatment)
  • Patients with respiratory failure, malignant tumors, or other autoimmune diseases

Lab values

  • 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)

Other

  • Patients with acute kidney injury
  • Patients who have undergone renal replacement treatment in the past
  • Women who are pregnant or breastfeeding at the time of enrollment or any time during the study

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chinese PLA General Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.