Exacerbating Factors in Inflammatory Bowel Disease

NCT ID: NCT01405105

Last Updated: 2014-02-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

134 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-08-31

Study Completion Date

2012-06-30

Brief Summary

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Cross-sectional study of potential triggers for flares of Crohn's disease or ulcerative colitis.

Detailed Description

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Detailed questionnaires with patient in regards to potential triggers for flares of IBD. Includes both patients with flares and those in remission as a control group.

Conditions

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Ulcerative Colitis Crohn's Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Patients with Flares of IBD

Active flare of Crohn's or UC

No interventions assigned to this group

Control Group

Patients with quiescent Crohn's disease or UC

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* History of verified Crohn's disease or ulcerative colitis

Exclusion Criteria

* unwilling to participate
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centocor Ortho Biotech Services, L.L.C.

INDUSTRY

Sponsor Role collaborator

Dallas VA Medical Center

FED

Sponsor Role lead

Responsible Party

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Linda A Feagins

Staff Gastroenterologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Linda A Feagins, MD

Role: PRINCIPAL_INVESTIGATOR

Dallas VA Medical Center

Locations

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Dallas VA Medical Center

Dallas, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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DVAMC-09-010

Identifier Type: -

Identifier Source: org_study_id

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