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Trials / Enrolling By Invitation

Enrolling By InvitationNCT06622187

Bleeding Prevention With Desmopressin for Allograft Kidney Biopsies

Bleeding Prevention With Desmopressin for Allograft Kidney Biopsies: a Double-blind Randomized Study

Status
Enrolling By Invitation
Phase
Phase 4
Study type
Interventional
Enrollment
96 (estimated)
Sponsor
Hospital de Clinicas de Porto Alegre · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to evaluate the efficacy and safety of desmopressin to prevent bleeding after percutaneous renal graft biopsy in patients at high risk of bleeding. Researchers will compare desmopressin (DDAVP) to placebo to see if the drug reduces the risk of bleeding events related to kidney biopsy. Participants will receive intravenous desmopressin medication (100ml) or placebo (100mL of saline solution) before the kidney biopsy.

Conditions

Interventions

TypeNameDescription
DRUGDesmopressin (DDAVP)Patients in the intervention group will receive desmopressin 0.3ug/kg administered as an intravenous infusion 1h before the proposed procedure
DRUGSodium ChloridePatients in the control group will receive sodium chloride 0.9% 100mL administered as an intravenous infusion 1h before the proposed procedure

Timeline

Start date
2024-08-14
Primary completion
2026-06-01
Completion
2026-06-14
First posted
2024-10-02
Last updated
2025-09-11

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT06622187. Inclusion in this directory is not an endorsement.