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Intensity Modulated Radiotherapy (IMRT) for the Pelvis Post-Hysterectomy

NCT00508703 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2017-09-12

No results posted yet for this study

Summary

The goal of this clinical research study is to use CT scans to find any changes in position of the vagina and pelvic lymph node areas during the course of IMRT radiation therapy. Treatment can then be adjusted in order to "spare" as much normal tissue as possible during radiation therapy. Another goal is to study the side effects of IMRT radiation therapy.

Conditions

Interventions

RADIATION

Intensity Modulated Radiotherapy (IMRT)

Dose of 45Gy

PROCEDURE

CT Scan

CT Scans: Twice a week during the 5 weeks of radiation treatment.

Sponsors & Collaborators

  • M.D. Anderson Cancer Center

    lead OTHER

Principal Investigators

  • Patricia J. Eifel, MD · M.D. Anderson Cancer Center

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-03-05
Primary Completion
2017-09-08
Completion
2017-09-08

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00508703 on ClinicalTrials.gov