Retroperitoneoscopic Donor Nephrectomy

Completed

• Conditions: Transplant; Complication, Failure

• Registration Number: NCT03893656
• Lead Sponsor: Samsun Liv Hospital

Brief Summary

to compare the results of right and left-sided retroperitoneoscopic donor nephrectomy (RDN).

Detailed Description

This was a retrospective study evaluating demographics, intraoperative and postoperative data of 158 kidney donors who underwent RDN from January 2010 to August 2018. Two groups were created according to the side of the surgery including Right RDN (group 1) and left RDN (group 2). The results of the recipients' were also evaluated.

Study Timeline

• Study Start: 2019-02-25
• Study First Submitted: 2019-03-24
• Study First Submitted QC: 2019-03-26
• Study First Posted: 2019-03-28
• Primary Completion: 2019-05-08
• Study Completion: 2019-07-22
• Status Verified: 2019-10
• Last Update Submitted: 2019-10-08
• Last Update Posted: 2019-10-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 158

Inclusion Criteria

• Adult donors
• Kidney donors undergoing retroperitoneoscopic donor nephrectomy
• Recipients of the kidneys
• Donors with the consent form
• Recipients with consent form

Exclusion Criteria

• open donor nephrectomies
• donors without the consent form
• Recipients without the consent form

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
incisional hernia	up to 2 years	abdominal incision or trocar site defects of donors
Blood loss	at the end of the surgery	amount of bleeding during surgery (mililiter)
postoperative complication	up to 1 month	abnormal problems that may be seen after surgery and require additional intervention or follow-up (grade I-V)
Operation time	at the end of the surgery	time from onset to complete of surgery
warm ishemia time	at the end of the surgery	time from renal artery and vein dissection of the kidney to the initiation of perfusion on the bench table.
İntraoperative complications	at the end of the surgery	abnormal problems that may be seen during surgery and require additional intervention.

Trial Locations

Locations (2)

Ondokuz Mayıs University; 🇹🇷 Samsun, Turkey

Samsun Liv Hospital; 🇹🇷 Samsun, Turkey