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COMPLETED
NCT07840313
NA

Prophylactic Desmopressin Before Native Kidney Biopsy in Severe Renal Impairment

Sponsor: Sindh Institute of Urology and Transplantation

View on ClinicalTrials.gov

Summary

This study evaluated whether giving desmopressin before a native kidney biopsy reduces bleeding complications in adults with severe renal impairment (eGFR \<30 mL/min/1.73 m²). Patients undergoing kidney biopsy were enrolled sequentially into two groups: a non-desmopressin group and a desmopressin group. Patients were monitored for 24 hours after biopsy for bleeding complications, including perinephric hematoma, a decrease in hemoglobin, blood in the urine, need for blood transfusion, and other complications. The study also evaluated whether desmopressin was associated with adverse effects such as low blood sodium levels.

Official title: Prophylactic Desmopressin and Bleeding Outcomes After Native Kidney Biopsy in Patients With Severe Renal Impairment: A Prospective Sequential Cohort Study

Key Details

Gender

All

Age Range

18 Years - 90 Years

Study Type

INTERVENTIONAL

Enrollment

250

Start Date

2017-08-01

Completion Date

2017-11-30

Last Updated

2026-09-25

Healthy Volunteers

No

Interventions

DRUG

Desmopressin Acetate

Prophylactic intranasal desmopressin acetate administered before native kidney biopsy in adults with severe renal impairment (eGFR \<30 mL/min/1.73 m²). Patients were monitored for 24 hours after biopsy for bleeding complications and safety outcomes.

OTHER

NO DESMOPRESSIN

Locations (1)

Sindh Institute of Urology and Transplantation (SIUT)

Karachi, Sindh, Pakistan