Quality of Life Following Radical Prostatectomy

This study is currently recruiting participants. (see Contacts and Locations)
Verified February 2014 by Stanford University
Sponsor:
Information provided by (Responsible Party):
Stanford University
ClinicalTrials.gov Identifier:
NCT00373308
First received: September 6, 2006
Last updated: February 12, 2014
Last verified: February 2014

September 6, 2006
February 12, 2014
September 2002
December 2015   (final data collection date for primary outcome measure)
  • urinary and bowel habits [ Time Frame: before and after surgery ] [ Designated as safety issue: No ]
  • sexual and hormonal index as self-reported in the questionnaires [ Time Frame: before and after surgery ] [ Designated as safety issue: No ]
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Complete list of historical versions of study NCT00373308 on ClinicalTrials.gov Archive Site
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Quality of Life Following Radical Prostatectomy
Quality of Life Following Radical Prostatectomy

This study will utilize the Expanded Prostate Cancer Index Composite questionnaire to learn what impact the surgery has upon the participant's sense of health, sexual and urinary quality of life.

To define impact on quality of life issues for patients undergoing radical prostatectomy. This study will distribute a questionnaire to patients who are being scheduled for radical prostatectomy, both before and after surgery, to assess the impact on quality of life issues. This will provide important information regarding the temporal return of issues pertaining to quality of life.

Observational
Observational Model: Cohort
Time Perspective: Retrospective
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Non-Probability Sample

Patients scheduled to undergo radical prostatectomy at Stanford

  • Prostatic Neoplasms
  • Prostate Cancer
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
200
December 2017
December 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

- Patients scheduled to undergo radical prostatectomy at Stanford

Exclusion Criteria:

- Patients treated with neoadjuvant or adjuvant hormonal therapy or radiation therapy

Male
18 Years and older
No
Contact: Ida Bezabeh 650-725-8057 ibezabeh@stanford.edu
United States
 
NCT00373308
PROS0012, 78463, PROS0012
Yes
Stanford University
Stanford University
Not Provided
Principal Investigator: Benjamin I Chung Stanford University
Stanford University
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP