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Completed No phase listed Observational

Quality of Life in Patients Undergoing Surgery or Brachytherapy for Stage II Prostate Cancer

ClinicalTrials.gov ID: NCT00052481

Public ClinicalTrials.gov record NCT00052481. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 4:16 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Health-Related Quality Of Life In Patients With Low Risk, Localized Prostate Cancer Randomized To Radical Prostatectomy Or Brachytherapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Quality of life assessment in patients undergoing prostate cancer treatment may help determine the intermediate-term and long-term effects of surgery and brachytherapy. PURPOSE: Randomized clinical trial to study quality of life in patients undergoing radical prostatectomy or brachytherapy for stage II prostate cancer.

Study identification

NCT ID
NCT00052481
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
500 participants

Conditions and interventions

Interventions

Procedure

Eligibility (public fields only)

Age range
Up to 75 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2002 (Type not available)
Primary completion
Apr 2004 (Actual)
Completion
Apr 2004 (Actual)
Last update posted
Jul 6, 2016

2002 – 2004

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
UCSF Comprehensive Cancer Center San Francisco California 94143-0128 —
Walter Reed Army Medical Center Washington D.C. District of Columbia 20307-5000 —
Holden Comprehensive Cancer Center at University of Iowa Iowa City Iowa 52242-1062 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Washington University School of Medicine St Louis Missouri 63110 —
Memorial Sloan-Kettering Cancer Center New York New York 10021 —
James P. Wilmot Cancer Center at University of Rochester Medical Center Rochester New York 14642 —
Presbyterian Hospital Charlotte North Carolina 28233-3549 —
Cleveland Clinic Taussig Cancer Center Cleveland Ohio 44195 —
Fletcher Allen Health Care - Medical Center Campus Burlington Vermont 05401 —
Sentara Norfolk General Hospital Norfolk Virginia 23507 —
University Cancer Center at University of Washington Medical Center Seattle Washington 98195-6043 —
Madigan Army Medical Center Tacoma Washington 98431-5048 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00052481, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 6, 2016 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00052481 live on ClinicalTrials.gov.

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