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

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
Victor Huynh, University of California, Irvine
ClinicalTrials.gov Identifier:
NCT00395564
First received: November 1, 2006
Last updated: June 24, 2013
Last verified: June 2013
  Purpose

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


Condition
Urologic Diseases

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Retrospective Chart Review of Patients Who Have Had an Open, Laparoscopic, Ureteroscopic or Percutaneous Surgery

Further study details as provided by University of California, Irvine:

Primary Outcome Measures:
  • Develop outcome effectiveness for minimally invasive procedures [ Time Frame: December 2015 ] [ Designated as safety issue: No ]

Estimated Enrollment: 150
Study Start Date: November 2008
Estimated Study Completion Date: December 2015
Estimated Primary Completion Date: December 2015 (Final data collection date for primary outcome measure)
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.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: Victor Huynh, Urology Account Contact, University of California, Irvine
ClinicalTrials.gov Identifier: NCT00395564     History of Changes
Other Study ID Numbers: 2008-6613
Study First Received: November 1, 2006
Last Updated: June 24, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, Irvine:
Urologic Surgery

Additional relevant MeSH terms:
Urologic Diseases

ClinicalTrials.gov processed this record on September 30, 2014