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Duke Urology Database and Specimen Bank

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00978991
First Posted: September 17, 2009
Last Update Posted: February 8, 2013
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):
Judd Moul, Duke University
  Purpose
The proposed project is aimed to build a Duke University-specific longitudinal urologic surgery database. It will be used as the main resource to support future research within Urology and Duke University.

Condition
Prostate Cancer Bladder Cancer Erectile Dysfunction Incontinence

Study Type: Observational
Study Design: Observational Model: Cohort
Official Title: Duke Longitudinal Urologic Surgery Patient Outcome Database

Resource links provided by NLM:


Further study details as provided by Judd Moul, Duke University:

Enrollment: 87820
Study Start Date: January 1988
Study Completion Date: November 2012
Primary Completion Date: November 2012 (Final data collection date for primary outcome measure)
Detailed Description:

Specifically, the database will be used for the following future studies. (i) To characterize the biomarkers/protein signature associated with urological diseases; (ii) To clarify the clinical role of the risk factors and their interactions for early detection and optimized treatment of urological diseases, and improvement of post-treatment quality of life; (iii) To develop algorithms and nomograms to accurately predict the outcome of urological diseases.

Retrospective review of subjects data prior to Institutional Review Board approval and prospective review of data on those consented after Institutional Review Board approval.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Urology
Criteria

Inclusion Criteria:

  • Duke Urology patients

Exclusion Criteria:

  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): NCT00978991


Locations
United States, North Carolina
Duke University Medical Center
Durham, North Carolina, United States, 27710
Sponsors and Collaborators
Duke University
Investigators
Principal Investigator: Judd W Moul, MD Duke University
  More Information

Responsible Party: Judd Moul, Professor of Surgery, Duke University
ClinicalTrials.gov Identifier: NCT00978991     History of Changes
Other Study ID Numbers: Pro00005140
First Submitted: September 15, 2009
First Posted: September 17, 2009
Last Update Posted: February 8, 2013
Last Verified: February 2013

Keywords provided by Judd Moul, Duke University:
Benign prostate hyperplasia
Erectile dysfunction

Additional relevant MeSH terms:
Urinary Bladder Neoplasms
Erectile Dysfunction
Urologic Neoplasms
Urogenital Neoplasms
Neoplasms by Site
Neoplasms
Urinary Bladder Diseases
Urologic Diseases
Sexual Dysfunction, Physiological
Genital Diseases, Male
Sexual Dysfunctions, Psychological
Mental Disorders