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COMPLETED

Vaginal Changes and Sexual Function in Patients With Cervical Cancer

NCT00053261 · View on ClinicalTrials.gov ↗

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

Sponsor

Gynecologic Oncology Group

61 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00053261

The ClinicalTrials.gov registry entry for NCT00053261 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. An enrollment target was not published in the registry record, which is common for early-stage or observational entries. The listed sponsor is Gynecologic Oncology Group, which has 61 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00053261 reports 12 study locations spanning 7 distinct geographic areas — top geographies include Michigan, New York, Oklahoma. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00053261?

The interventions under investigation include: management of therapy complications (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00053261?

This trial is sponsored by Gynecologic Oncology Group, which has 61 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial