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Clinical Trials in Turkey / NCT07823387
Recruiting Observational

Intra-Abdominal Pressure Changes During Continuous Renal Replacement Therapy in Critically Ill Patients

NCT07823387 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-07-20
Last updated
2026-09-16

Condition(s) studied

Intra-Abdominal HypertensionCritical IllnessContinuous Renal Replacement Therapy

Investigational drug(s) / intervention(s)

Intravesical Intra-abdominal Pressure Measurement

Intravesical Intra-abdominal Pressure Measurement: Intravesical intra-abdominal pressure will be measured via the existing urinary catheter at baseline and at 6, 12, 24, 48, and 72 hours after initiation of continuous renal replacement therapy (CRRT). Measurements will be performed for study data collection only. No therapeutic intervention or modification of routine clinical management will be undertaken based solely on the study measurements.

Study summary

This prospective observational study will evaluate changes in intra-abdominal pressure in critically ill adult patients receiving continuous renal replacement therapy in the intensive care unit. Intra-abdominal pressure will be measured through the urinary bladder at predefined time points during therapy. The study will also assess the relationship between intra-abdominal pressure changes and clinical variables, including fluid balance, hemodynamic parameters, vasopressor requirement, urine output, severity scores, duration of renal replacement therapy, intensive care unit and hospital length of stay, and 30-day survival. No additional treatment or therapeutic intervention will be administered for research purposes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older * Admission to the intensive care unit * Receiving continuous renal replacement therapy (CRRT) * Presence of an indwelling urinary (Foley) catheter for intra-abdominal pressure measurement Exclusion Criteria: * Pregnancy * Open abdominal wound or open abdomen * Neurogenic bladder * History of bladder surgery * Pelvic hematoma * Pelvic fracture * Presence of an intra-abdominal mass or other anatomical/technical condition that may compromise the reliability of intravesical pressure measurement

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
SBÜ Bursa Yüksek İhtisas Eğitim ve Araştırma Hastanesi Bursa Bursa Recruiting

More Bursa Yuksek Ihtisas Training and Research Hospital trials in Turkey

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 NCT07823387 on ClinicalTrials.gov ↗ ← All trials in Turkey