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Renal Donor Comparison of Outcomes: Hand Assist Versus Laparoscopic Nephrectomy

This study has been withdrawn prior to enrollment.
(Principal Investigator left institution)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00460889
First Posted: April 17, 2007
Last Update Posted: April 6, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Columbia University
  Purpose
This study is designed to look at outcomes of patients who have undergone hand assisted laparoscopic donor nephrectomy versus totally laparoscopic donor nephrectomy.

Condition Intervention
Living Renal Donor Procedure: donor nephrectomy

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Renal Donor Comparison of Outcomes: Hand Assist Versus Laparoscopic Nephrectomy

Further study details as provided by Columbia University:

Primary Outcome Measures:
  • Prevalence of postoperative comfort and hospital stay satisfaction with HALDN [ Time Frame: 1 week ]
  • Prevalence of postoperative comfort and hospital stay satisfaction with LDN [ Time Frame: 1 week ]

Enrollment: 0
Study Start Date: October 2006
Study Completion Date: August 2008
Primary Completion Date: August 2008 (Final data collection date for primary outcome measure)
Intervention Details:
    Procedure: donor nephrectomy
    The objective of this protocol is to look at the outcomes of laparoscopic donor nephrectomy performed by using hand assisted (HA)or entirely laparoscopic (LDN) surgical techniques. To define the advantages of each technique, we will use records of patients who underwent laparoscopic live kidney donation with HALDN.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Surgical clinic
Criteria

Inclusion Criteria:

  • any person undergoing minimally invasive donor nephrectomy surgery at NewYork Hospital/Columbia.

Exclusion Criteria:

  • any person undergoing open donor nephrectomy surgery at NewYork Hospital/Columbia.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00460889


Locations
United States, New York
Columbia University College of Physicians and Surgeons
New York, New York, United States, 10032
Sponsors and Collaborators
Columbia University
Investigators
Principal Investigator: Dennis L Fowler, MD Columbia University
  More Information

Responsible Party: Columbia University
ClinicalTrials.gov Identifier: NCT00460889     History of Changes
Other Study ID Numbers: AAAB9478
First Submitted: April 13, 2007
First Posted: April 17, 2007
Last Update Posted: April 6, 2015
Last Verified: April 2015

Keywords provided by Columbia University:
hand assist
laparoscopy
renal donor
outcomes