Evaluation of Hemostatic Agents in Partial Nephrectomy: A Prospective Randomized Trial

Completed Not Applicable NCT07232927

Study Description

This prospective randomized study aims to evaluate the effect of adjunctive hemostatic agents (FloSeal® and Surgicel®) on perioperative outcomes in patients undergoing partial nephrectomy for localized renal tumors. A total of 150 patients were randomized into three groups: standard parenchymal suturing (Group A), suturing with FloSeal® (Group B), and suturing with Surgicel® (Group C). The study primarily investigates whether hemostatic agents reduce postoperative hemorrhage, urinary leakage, and positive surgical margin rates. Secondary outcomes include renal function change, operative and ischemia times, estimated blood loss, and hospital stay. All surgeries were performed by a single experienced surgeon at Ankara University Urology Department between January 2023 and December 2024.

Study Details

Registry ID:
NCT07232927
Conditions:
Partial Nephrectomy, Hemostatic Agents, Localized Renal Cell Carcinoma
Phase:
Not Applicable
Target Enrollment:
150 participants
Start Date:
Age Range:
18–999 years
Healthy Volunteers:
No

Study Locations (1 site)

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