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Clinical Trials in Poland / NCT07746102
Recruiting Not applicable

Assessment of the Impact of Repeated Ischemic Preconditioning Episodes on Hemodynamic and Metabolic Parameters in Patients at Various Stages of Chronic Kidney Disease

NCT07746102 · tracked via the Priya Life Science Poland tracker
Phase
Not applicable
Started
2026-07-23
Last updated
2026-08-04

Condition(s) studied

HemodialysisIschemia PreconditioningChronic Kidney DiseaseBlood Pressure DisordersInflammation

Investigational drug(s) / intervention(s)

Preconditioning with control ischemic episodes

Preconditioning with control ischemic episodes: 4 cycles of 5-minute inflation and deflation using a sphygmomanometer cuff at a pressure of 30 mmHg above the systolic value through three consecutive days

Study summary

The aim of our study is to evaluate the impact of repeated episodes of ischemic quenching on changes in blood pressure, heart rate and laboratory parameters of inflammation in patients with kidney diseases. There is credible evidence that intentionally producing periods of ischemia provides protection of the myocardium and blood vessels against subsequent ischemic injury. The examination will be performed during hospitalization in the Department of Nephrology, Hypertension, Transplantology and Internal Diseases and will last 4 days. On the first day, blood pressure will be measured using an automatic blood pressure monitor, radial artery pulse, blood saturation will be measured using a pulse oximeter, and approximately 6 ml of venous blood will be collected from the elbow bend area for laboratory tests. Then, compression of the lower limb below the knee will be performed using a blood pressure cuff. Four 5-minute cycles of inflation and deflation of the cuff will be performed. The pressure on the lower limb will be repeated on the next two days. On the last day of the examination, blood pressure, heart rate and blood saturation will be measured again, and approximately 6 ml of venous blood will be collected again for laboratory tests.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * obtaining the patient's voluntary, informed consent to participate in the experiment, * chronic kidney disease in stages G1-G5, * women and men over 18 years of age. * failure to meet the qualification criteria for participation in the study, * consciousness disorders, * heart failure (NYHA IV), * severe anemia (Hb concentration\<8g/dL), * features of muscle cell damage (e.g. rhabdomyolysis), * peripheral circulation disorders, peripheral vascular diseases. Exclusion Criteria: \-

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Medical University of Lodzi Lodz Poland Recruiting
Medical University of Lodzi Lodz Poland Recruiting

More Medical University of Lodz trials in Poland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07746102 on ClinicalTrials.gov ↗ ← All trials in Poland