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NCT00648635Active, not recruiting

Relationship Between Quality of Life, Treatment Modalities, and Patient Treatment/Outcome Expectations

A Pilot Study for Prospective Discovery of Possible Relationship Between Quality of Life, Treatment Modalities, and Patient Treatment/Outcome Expectations in Patients Undergoing Treatment for Locally Recurrent Rectal Adenocarcinoma

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

The goal of this study is to learn how the treatment given to patients with recurrent rectal cancer affects their well being and quality of life.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
116 (actual)
First submitted
27 Mar 2008
Start date
12 Mar 2008
Primary completion date
30 Sept 2027
Lead sponsor
M.D. Anderson Cancer Center
NCT number
NCT00648635

What you commit to

  • Study type: Observational
  • Participants enrolled: 116
  • From 12 Mar 2008 to the primary completion date, 30 Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients must not have any concurrent pelvic malignancy in addition to rectal carcinoma.
  • Patient must not have had solely non-operative therapies in treatment of their primary rectal carcinoma.

Other illness

  • Patients must not have a history of either a documented pelvic pain syndrome or a preoperative documented diagnosis of chronic constipation (defined as \< 1 BM per 48 hours, unrelated to rectal cancer or mechanical obstruction) preceding the cancer diagnosis.

Other

  • Patients must not have non-adenocarcinoma pathology, i.e., squamous cell carcinoma of the anus, cloacogenic tumors, etc.
  • Patients must not have ONLY distant metastases. Recurrence must be present within the bony pelvis.

Who the study is looking for

  • All patients who have had previous surgical treatment of rectal adenocarcinoma, regardless of age, with locally recurrent (pelvic) rectal adenocarcinoma are eligible, if a period of at least 3 months exists between initial treatment and disease recurrence.
  • Patients may have local recurrence alone, or concurrent distant metastatic disease. Patients must have recurrent rectal cancer present in the bony pelvis.
  • Patients must be conversant in English in order to complete appropriate questions.
  • Patients must understand the test and questionnaire parameters, including the need for PET testing to assess the correlation between perceived symptoms and PET or other diagnostic results. Patients must be able and willing to complete all scheduled appointments and complete and return all study questionnaires.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Texas - MD Anderson Cancer Center
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.