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RECRUITING
NCT05467033
PHASE3

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

Sponsor: Medical University of Bialystok

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

424

Start Date

2022-09-01

Completion Date

2026-08-31

Last Updated

2025-05-08

Healthy Volunteers

No

Conditions

Interventions

DRUG

Desmopressin

desmopressin 0,3ug/kg in 100ml 0,9% NaCl managed as intravenous infusion;

DRUG

intravenous infusion NaCl

0,9% NaCl managed as intravenous infusion

Locations (1)

II Department of Nephrology and Hypertension

Bialystok, Poland