Prospective Assessment of Symptoms and Quality of Life in Rectal Cancer Patients Receiving Chemo-Radiotherapy
Completed
Conditions studied: Rectal Cancer
In brief
Prospective Assessment of Symptoms and Quality of Life in Rectal Cancer Patients Receiving Chemo-Radiotherapy.
Key facts
- Study ID
- NCT00414232
- Run by
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- People needed
- 13
- Starts
- 2006-11-01
- Expected to finish
- 2010-10-01
- Last updated by the study team
- 2019-11-26
Who can join
Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- All of the following questions must be answered "yes" for a patient to be eligible for this protocol.
- Is there a working diagnosis of rectal cancer? YES NO
- Will the patient be receiving neoadjuvant concurrent chemotherapy and pelvic radiation? YES NO
- Is the pelvic radiation planned for a dose of 45-54 Gy and will it be delivered using a standard 3-field technique? YES NO
- Is the patient ≥ 18 years of age? YES NO
- Can the patient give informed consent? YES NO
You may not qualify if…
- All of the following questions must be answered "no" for a patient to be eligible for this protocol.
- Has there been prior radiation to the pelvis? YES NO
- Is the patient in the "special category" designated by the Public Health Service (patients younger than 18, pregnant women, and prisoners)? YES NO
Where it is running
- The Sidney Kimmel Comprehensive Cancer Center at The Johns Hopkins University — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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