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Laparoscopic Donor Nephrectomy clinical trials

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NCT ID: NCT02805517 Terminated - Clinical trials for Laparoscopic Donor Nephrectomy

Port Site Pain Following Percutaneous Externally-Assembled Laparoscopic Donor Nephrectomy

Start date: July 11, 2016
Phase: N/A
Study type: Interventional

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