Retroperitoneoscopic Donor Nephrectomy

Retroperitoneoscopic Donor Nephrectomy: a Retrospective Single-center Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03893656

Acronym

RDN

Enrollment

158

Registered

2019-03-28

Start date

2019-02-25

Completion date

2019-07-22

Last updated

2019-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transplant; Complication, Failure

Keywords

Living donor nephrectomy, Kindey transplantation, Retroperitoneoscopic donor nephrectomy, Hernia

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 57 Years

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

Design outcomes

Primary

Measure	Time frame	Description
Operation time	at the end of the surgery	time from onset to complete of surgery
Blood loss	at the end of the surgery	amount of bleeding during surgery (mililiter)
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.
incisional hernia	up to 2 years	abdominal incision or trocar site defects of donors
postoperative complication	up to 1 month	abnormal problems that may be seen after surgery and require additional intervention or follow-up (grade I-V)

Countries

Turkey (Türkiye)

Outcome results