drugset / Trial / NCT05467033

Safety Outcomes Post Kidney Biopsy - Randomized Clinical Evaluation of Efficacy of Desmopressin

NCT05467033

Phase 3 Recruiting 424 enrolled Medical University of Bialystok
RandomizedParallel-groupTriple-blindPrevention

Summary

It is a randomized, multicenter, double-blind, placebo controlled, interventional clinical trial that will be conducted in Poland, in about 6 Hospital Nephrology Departments to evaluate the safety and effectiveness of desmopressin on the prevention of bleeding after percutaneous needle kidney biopsy in patients with rare and ultrarare glomerulonephritis.

Timeline

Start
2022-09-01
Primary completion
2026-08-31
Completion
2026-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Desmopressin Peptide 0.3 ug/kg Intravenous

Indications

No indication recorded.