Status:
COMPLETED
Post-Op Quality of Life After Colorectal Surgery
Lead Sponsor:
University Hospitals Cleveland Medical Center
Conditions:
Colorectal Neoplasms
Colitis, Ulcerative
Eligibility:
All Genders
18-85 years
Brief Summary
The purpose of this study is to produce a user-friendly tool- in the form of a questionnaire - to accurately assess early quality of life in patients after abdominal colorectal surgery from the first ...
Detailed Description
The purpose of this study is to produce a user-friendly tool to accurately assess early quality of life in postoperative patients following abdominal colorectal surgery in the early postoperative peri...
Eligibility Criteria
Inclusion
- Subjects who are 18 years of age and older
- Subjects of either sex
- Subjects who will undergo any colorectal abdominal surgery at University Hospitals of Cleveland
- Subjects who agree to participate in the study program and provide written informed consent
- Diagnoses of Crohn's disease, ulcerative colitis, rectal or colon cancer, colon or rectal polyps and diverticulitis
Exclusion
- Patients in the middle of three part surgery or had recent surgery (i.e., back for stoma closure for J-pouch)
- Patients with diagnosis of rectal prolapse, condyloma or any other condition that cannot be performed abdominally with an open or laparoscopic procedure
- Patient who have undergone major surgery within the month prior to this colorectal surgery
- Pregnant women, minors, psychiatric patients and prisoners
Key Trial Info
Start Date :
October 1 2005
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 1 2008
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00468455
Start Date
October 1 2005
End Date
May 1 2008
Last Update
December 15 2014
Active Locations (1)
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1
University Hospitals of Cleveland
Cleveland, Ohio, United States, 44106