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Chart Review of Those Who Have Had Open, Laparoscopic, Ureteroscopic, or Percutaneous Surgery

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ClinicalTrials.gov Identifier: NCT00395564
Recruitment Status : Completed
First Posted : November 3, 2006
Last Update Posted : December 14, 2016
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
The investigator intends to review retrospective de-identified data of patients who have had Open, Laparoscopic, Ureteroscopic or Percutaneous Urologic Surgery.

Condition or disease
Urologic Diseases

Detailed Description:
The investigator reviews retrospective de-identified data of patients who have had Open, Laparoscopic, Ureteroscopic or Percutaneous Urologic Surgery in order to determine different clinical or operative issues.

Study Design

Study Type : Observational
Estimated Enrollment : 150 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Retrospective Chart Review of Patients Who Have Had an Open, Laparoscopic, Ureteroscopic or Percutaneous Surgery
Study Start Date : November 2008
Primary Completion Date : November 2011
Study Completion Date : November 2011
Groups and Cohorts


Outcome Measures

Primary Outcome Measures :
  1. Develop outcome effectiveness for minimally invasive procedures [ Time Frame: December 2015 ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Those who have urologic conditions that need to be treated with open, laparoscopic, ureteroscopic, or percutaneous urologic surgery.
Criteria

Inclusion Criteria:

  • Patients must have had Open, Laparoscopic, Ureteroscopic or Percutaneous Urologic Surgery at UCIMC Department of Urology
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): NCT00395564


Locations
United States, California
University of California, Irvine Medical Center
Orange, California, United States, 92868
Sponsors and Collaborators
University of California, Irvine
Investigators
Principal Investigator: Elspeth McDougall University of California Irvine-Department of Urology
More Information

Responsible Party: Jaime Landman, Professor and Chairman, University of California, Irvine
ClinicalTrials.gov Identifier: NCT00395564     History of Changes
Other Study ID Numbers: 2008-6613
First Posted: November 3, 2006    Key Record Dates
Last Update Posted: December 14, 2016
Last Verified: December 2016

Keywords provided by Jaime Landman, University of California, Irvine:
Urologic Surgery

Additional relevant MeSH terms:
Urologic Diseases