Ileal Pouch-Anal Anastomosis Registry
Stopped early
Conditions studied: Ileal Pouch-Anal Anastomosis
In brief
Little is known about the factors that predispose patients to complications after an ileal pouch-anal anastomosis procedure (IPAA). Our goal is to establish a registry that prospectively captures pre- and post-surgical data from participants. Retrospective studies concerning IPAA outcomes and will be conducted using these data.
Key facts
- Study ID
- NCT01026480
- Run by
- Boston Medical Center
- People needed
- 936
- Starts
- 2009-11-01
- Expected to finish
- 2017-03-16
- Last updated by the study team
- 2017-03-17
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with one of the following: Ulcerative colitis, Crohn's disease, Indeterminate colitis, Familial adenomatous polyposis, Hereditary nonpolyposis colorectal cancer, Lynch syndrome I or II, or Gardners' syndrome
- Treated by a Center for Digestive Disorders physician
- Scheduled for, or has undergone, ileal pouch-anal anastomosis procedure
You may not qualify if…
- Patients who do not speak a language for which the IRB has approved an Informed Consent Form or Short Form
- Patients who are currently incarcerated
Where it is running
- Boston Medical Center — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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