Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00053261 · ClinicalTrials.gov registry record

Vaginal Changes and Sexual Function in Patients With Cervical Cancer

A clinical trial of Cervical Cancer and Sexuality and Reproductive Issues, sponsored by Gynecologic Oncology Group.

Completed
Registry status
12
Study locations

NCT00053261: Completed study of Cervical Cancer and Sexuality and Reproductive Issues, sponsored by Gynecologic Oncology Group.

NCT00053261 is a study of Cervical Cancer and Sexuality and Reproductive Issues that has completed, run by Gynecologic Oncology Group. The trial reports 12 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00053261, a study of Cervical Cancer and Sexuality and Reproductive Issues, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
12
Study locations

Study Summary

RATIONALE: Vaginal changes that may effect sexual function occur in patients undergoing treatment for cervical cancer. PURPOSE: Clinical trial to determine the type of vaginal changes such as vaginal dryness that occur in patients receiving treatment for cervical cancer and the effect these changes have on sexual function.

Interventions

  • PROCEDURE management of therapy complications

Study Locations (12)

Michigan

  • Bronson Methodist Hospital - Kalamazoo
  • West Michigan Cancer Center - Kalamazoo
  • Borgess Medical Center - Kalamazooaa

New York

  • Long Island Cancer Center at Stony Brook University Hospital - Stony Brook
  • SUNY Upstate Medical University Hospital - Syracuse

Oklahoma

  • Oklahoma University Medical Center - Oklahoma City
  • Cancer Care Associates - Midtown Tulsa - Tulsa

Pennsylvania

  • Abington Memorial Hospital - Abington
  • John and Dorothy Morgan Cancer Center at Lehigh Valley Hospital - Allentown

Georgia

  • Curtis & Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center - Savannah

Missouri

  • Ellis Fischel Cancer Center at University of Missouri - Columbia - Columbia

North Carolina

  • Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill - Chapel Hill

Trial Details

FieldValue
Start Date 2003-07
Gynecologic Oncology Group

154 total trials

What the finished NCT00053261 record still lists

NCT00053261 is an observational study that tracks outcomes without assigning an intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.

The record links to 2 conditions, with Cervical Cancer appearing as the primary indexed condition, and to 1 intervention - of which management of therapy complications is the first listed.

NCT00053261 lists 12 locations in 7 states (Michigan, New York, Oklahoma).

Frequently Asked Questions

What is clinical trial NCT00053261 about?

NCT00053261 is a clinical study titled "Vaginal Changes and Sexual Function in Patients With Cervical Cancer". RATIONALE: Vaginal changes that may effect sexual function occur in patients undergoing treatment for cervical cancer. PURPOSE: Clinical trial to determine the type of vaginal changes such as vaginal dryness that occur in patients receiving treatment for cervical cancer and the effect these changes...

What is the current status of trial NCT00053261?

This trial is currently completed. The study started on 2003-07.

What conditions does trial NCT00053261 study?

This clinical trial studies the following conditions: Cervical Cancer, Sexuality and Reproductive Issues.

What interventions are being tested in trial NCT00053261?

The interventions under investigation include: management of therapy complications (PROCEDURE).

Who is sponsoring clinical trial NCT00053261?

This trial is sponsored by Gynecologic Oncology Group, which has 154 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00053261 being conducted?

This trial has 12 study locations across Georgia, Michigan, Missouri, New York, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00053261, the US trial registry maintained by the National Library of Medicine. NCT00053261 (unsized enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.