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Completed No phase listed Observational

Study to Determine Risk Factors for Post-operative Infection in Inflammatory Bowel Disease

ClinicalTrials.gov ID: NCT02054533

Public ClinicalTrials.gov record NCT02054533. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 7:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective Cohort of Ulcerative Colitis and Crohn's Disease Patients Undergoing Surgery to Identify Risk Factors for Post-Operative Infection I

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Understanding of how best to treat inflammatory bowel disease (IBD) has evolved over the last ten years. Evidence now suggests that the most effective therapy early in the course of Crohn's disease (CD) and ulcerative colitis (UC) involves the use of immune suppressing medications such as the anti-Tumor Necrosis Factor (anti-TNF) agents infliximab, adalimumab, and certolizumab. However, many CD and UC patients still ultimately require surgery despite the use of these medications. Side effects of the anti-TNF agents include increased risk of infections due to their effect on the immune system. Little is known about how use of these medications near the time of surgery may affect patients' risks of infection or other post-operative complications. The only available studies on this topic have given conflicting results. These studies have been limited by the fact that they have been small in size and retrospective. Retrospective studies primarily involve chart review as the method of identifying potential risk factors for infections and other complications after they have already occurred. This method limits both the type and quality of information/data that can be collected. The conflicting results have led to variance in practice patterns with regards to management of anti-TNF agents, the timing of surgery, and even the types of surgery. By enrolling patients at the time of their surgery, collecting extensive information may be possible than previously studied on potential risk factors for both infectious and non-infectious complications following surgery. Risk factors to be studied will include individual patient characteristics, disease characteristics, surgical methods, novel characteristics of CT scans and MRIs and extensive medication exposures. The primary objective is to determine if exposure to anti-TNF agents prior to surgery increases the risk of infection post-operatively. And evaluate exposure to anti-TNF agents by both patient history of use and measurement of anti-TNF drug levels at the time of surgery. Monitoring of drug levels at the time of surgery has never been utilized in this way to evaluate the risk of anti-TNF agents in IBD. However, this has been done to assess the risk of other medications in different diseases. If anti-TNF agents are found to pose a risk for infectious or non-infectious outcomes in IBD patients undergoing surgery, change maybe needed in the way these medications are used around the time of surgery. Additionally, by collecting comprehensive information on other potential risk factors besides medication use patients at greatest risk for bad outcomes can be identified and take protective measures when possible. The aims of this study address the CCFA challenge to better define the risks of medical and surgical therapies to improve the quality of care of IBD patients undergoing surgery.

Study identification

NCT ID
NCT02054533
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
974 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2014
Primary completion
Jun 29, 2017
Completion
Jun 29, 2017
Last update posted
Sep 12, 2017

2014 – 2017

United States locations

U.S. sites
24
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Mayo Clinic Arizona Scottsdale Arizona 85259
Cedars-Sinai Medical Center Los Angeles California 90048
University of California San Francisco San Francisco California 94115
University of Colorado Anschutz Medical Campus Aurora Colorado 80045
University of Florida College of Medicine Gainesville Florida 32608
Cleveland Clinic Florida Weston Florida 33331
The University of Chicago Chicago Illinois 60637
Carle Foundation Hospital Urbana Illinois 61801
University of Maryland School of Medicine Baltimore Maryland 21201
Massachusetts General Hospital Boston Massachusetts 02114
Brigham and Women's Hospital, Inc. Boston Massachusetts 02115
Boston Medical Center Boston Massachusetts 02118
University of Michigan Ann Arbor Michigan 48109
Mayo Clinic Rochester Rochester Minnesota 55905
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
Icahn School of Medicine at Mount Sinai New York New York 10021
Lenox Hill Hospital New York New York 10028
University of North Carolina Chapel Hill North Carolina 27599
Wake Forest School of Medicine Winston-Salem North Carolina 27157
University Hospitals Case Medical Center Cleveland Ohio 44106
Cleveland Clinic Cleveland Ohio 44195
Penn State College of Medicine Hershey Pennsylvania 17033
The University of Pennsylvania Philadelphia Pennsylvania 19104
University of Pittsburth Pittsburgh Pennsylvania 15213

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02054533, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 12, 2017 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02054533 live on ClinicalTrials.gov.

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