- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01033682
Evaluation of Bladder Volumes in Patients Receiving Radiotherapy to the Rectum, Using Kilovoltage Cone-beam Imaging (FILL)
December 15, 2009 updated by: Royal Marsden NHS Foundation Trust
The purpose of this study is to implement and access a newly developed bladder filling protocol for patients receiving radiotherapy for rectal cancer using imaging on the treatment unit.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
10
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Surrey
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Sutton, Surrey, United Kingdom, SM2 5PT
- Recruiting
- Royal Marsden NHS Foundation Trust
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients receiving radiotherapy to the rectum
Description
Inclusion Criteria:
- Patients receiving radical radiotherapy to rectal malignancies.
- Age > 18 years old
- No previous lower GI radiotherapy
- Written informed consent according to good clinical practice (GCP) and national / local regulations.
Exclusion Criteria:
- Patients receiving palliative radiotherapy to rectal malignancies.
- Patients receiving radical short course preoperative radiotherapy for rectal malignancies.
- Patients unable to give informed consent.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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The percentage of patients who are able to achieve a bladder volume within +/- 30% of planning volume, on all treatment CBCT (cone beam computed tomography) scans
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Secondary Outcome Measures
Outcome Measure |
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The per-patient standard deviation of bladder volume throughout the course of radiotherapy
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The percentage of patients who are unable to follow the bladder filling protocol at any point during their treatment.
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The correlation between bladder volume and small bowel volume planning target volume
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Dr Diana Tait, Royal Marsden NHS Foundation Trust
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2009
Primary Completion (Anticipated)
February 1, 2010
Study Completion (Anticipated)
February 1, 2010
Study Registration Dates
First Submitted
December 15, 2009
First Submitted That Met QC Criteria
December 15, 2009
First Posted (Estimate)
December 16, 2009
Study Record Updates
Last Update Posted (Estimate)
December 16, 2009
Last Update Submitted That Met QC Criteria
December 15, 2009
Last Verified
December 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CCR3175
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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