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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00585728
Other study ID # 2007-0134 (CC07206)
Secondary ID A534260SMPH\MEDI
Status Completed
Phase N/A
First received
Last updated
Start date September 2007
Est. completion date August 2011

Study information

Verified date August 2011
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see how CT virtual proctoscopy compares to an ultrasound exam of the rectal area in determining the stage of rectal cancer for people recently diagnosed with rectal cancer. This study will also compare tumor volume before and after neoadjuvant therapy using CT virtual proctoscopy, with the ultrasound exam as a comparison. Neoadjuvant therapy consists of chemotherapy and radiation therapy. Neoadjuvant chemoradiation therapy is done before surgery to reduce the size of tumors.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients who have been diagnosed with adenocarcinoma of the rectum, who have not started their neoadjuvant treatment yet.

Exclusion Criteria:

- Patients who have started their neoadjuvant therapy already

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
CT Virtual Proctoscopy (CTVP)
CTVP done prior to initiation of therapy and a couple of weeks before patient has surgery.

Locations

Country Name City State
United States University of Wisconsin Hospital & Clinics Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The utility of CT virtual proctoscopy (CTVP) for evaluation of rectal cancer. 3 months
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