Port Site Pain Following Percutaneous Externally-Assembled Laparoscopic Donor Nephrectomy

Stopped early · Not applicable

Conditions studied: Laparoscopic Donor Nephrectomy

In brief

A single-arm prospective internally-controlled study. Patients will undergo Percutaneous Externally-Assembled Laparoscopic (PEAL) donor nephrectomy where one or more 3 mm instruments are added or substituted for conventional 5 or 12 mm trocars. Multiple outcome measures (endpoints) will be measured including time to first opioid use, total inpatient opioid dosage, patient ranking of painfulness of each port site, duration of ileus, time to ambulation, length of hospital stay, presence of any intraoperative or postoperative complications, operating time, estimated blood loss, and other routine parameters collected in a prospective surgical study

Key facts

Study ID

NCT02805517

Run by

Loma Linda University

People needed

6

Starts

2016-07-11

Expected to finish

2021-05-26

Last updated by the study team

2022-12-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing laparoscopic donor nephrectomy

You may not qualify if…

• Patients unwilling to participate in the study
• Patients unfit for laparoscopic surgery

Where it is running

• Loma Linda Medical Center — Loma Linda, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.