- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00634153
The Surgical Gastrointestinal Diseases Registry Protocol
February 15, 2018 updated by: Randall Brand, University of Pittsburgh
By placing the medical record information of many subjects into a research registry, researchers will be able to conduct research studies directed at increasing our knowledge about Gastrointestinal Diseases.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Researchers are asking for past, current and future medical record information.
Study Type
Observational
Enrollment (Actual)
750
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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Pennsylvania
-
Pittsburgh, Pennsylvania, United States, 15232
- University of Pittsburgh Cancer Institute
-
-
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 with gastrointestinal diseases.
Description
Inclusion Criteria:
- Subjects being seen by the University of Pittsburgh Medical Center for gastrointestinal diseases
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Allow researchers to review and study the medical records of many individuals to answer questions about their disease and its treatment.
Time Frame: 1-N/A
|
1-N/A
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
It will help researchers identify and recruit subjects who are eligible for participation in future research studies.
Time Frame: 1-N/A
|
1-N/A
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Randall E. Brand, MD, University of Pittsburgh
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
January 1, 2004
Primary Completion (Actual)
January 30, 2018
Study Completion (Actual)
January 30, 2018
Study Registration Dates
First Submitted
March 3, 2008
First Submitted That Met QC Criteria
March 11, 2008
First Posted (Estimate)
March 12, 2008
Study Record Updates
Last Update Posted (Actual)
February 19, 2018
Last Update Submitted That Met QC Criteria
February 15, 2018
Last Verified
February 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 03-145
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.