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Search / Trial NCT03251118

A 5-year Longitudinal Observational Study of Patients Undergoing Therapy for Inflammatory Bowel Disease

Launched by TARGET PHARMASOLUTIONS, INC. · Aug 11, 2017

Trial Information

Current as of July 25, 2025

Recruiting

Keywords

Crohn's Disease Ulcerative Colitis Indeterminate Colitis Digestive System Diseases

ClinConnect Summary

The TARGET-IBD study is a 5-year research project looking at patients with Inflammatory Bowel Disease (IBD), which includes conditions like Crohn's disease, ulcerative colitis, and indeterminate colitis. This study aims to gather information about how well current and future treatments for IBD work in real-life settings, both in hospitals and community clinics. It will track the safety and effectiveness of these therapies over time, helping to improve care for people with IBD.

To participate, individuals must be at least 2 years old and have been diagnosed with one of the IBD conditions. They should also be receiving treatment for their condition outside of a clinical trial and plan to continue follow-up visits for their IBD care. Participants will be asked to share their experiences and medical information during the study, which could help doctors understand more about managing IBD in everyday practice. It's important to note that those who are involved in other treatment studies or have had a total removal of the colon for ulcerative colitis are not eligible for this study.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Adults and children (age 2 or older) with a diagnosis of Crohn's disease (CD), Ulcerative colitis (UC), or Indeterminate colitis (IBDU) having been prescribed any IBD treatment (initial or subsequent) outside of a clinical trial.
  • 2. Have plans for future visits at the site for continued management of IBD.
  • Exclusion Criteria:
  • 1. Inability to provide written informed consent/assent.
  • 2. Being enrolled in any interventional study or trial for IBD treatment. Note: Patient may be enrolled in other registries or studies where IBD treatment outcomes are observed and/or reported (such as center-based registries).
  • 3. Prior total abdominal colectomy for UC or IBDU.

About Target Pharmasolutions, Inc.

Target Pharmasolutions, Inc. is a leading clinical trial sponsor dedicated to advancing pharmaceutical research and development. With a focus on innovative solutions, the company specializes in providing comprehensive clinical trial management services that enhance the efficiency and effectiveness of drug development. Target Pharmasolutions leverages cutting-edge technology and a team of experienced professionals to ensure regulatory compliance and optimize patient engagement, ultimately facilitating the successful delivery of new therapies to market. Committed to quality and integrity, the company partners with biopharmaceutical organizations to support their clinical goals and drive transformative outcomes in healthcare.

Locations

Minneapolis, Minnesota, United States

Houston, Texas, United States

Philadelphia, Pennsylvania, United States

Iowa City, Iowa, United States

Stanford, California, United States

Omaha, Nebraska, United States

Saint Louis, Missouri, United States

Nashville, Tennessee, United States

Dallas, Texas, United States

Ann Arbor, Michigan, United States

Seattle, Washington, United States

Mission Hills, California, United States

Aurora, Colorado, United States

Indianapolis, Indiana, United States

Chicago, Illinois, United States

Sacramento, California, United States

Winston Salem, North Carolina, United States

Baton Rouge, Louisiana, United States

Bronx, New York, United States

Columbus, Ohio, United States

Poughkeepsie, New York, United States

Palm Harbor, Florida, United States

New York, New York, United States

Shreveport, Louisiana, United States

Chapel Hill, North Carolina, United States

Tacoma, Washington, United States

Lancaster, California, United States

Madison, Wisconsin, United States

New York, New York, United States

Clearwater, Florida, United States

Jacksonville, Florida, United States

Atlanta, Georgia, United States

Lebanon, New Hampshire, United States

New Brunswick, New Jersey, United States

Cary, North Carolina, United States

Charlotte, North Carolina, United States

Cleveland, Ohio, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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