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VEST: The UK Vedolizumab Real Life Experience Study in Inflammatory Bowel Disease

U

University Hospital Southampton NHS Foundation Trust

Status

Unknown

Conditions

Ulcerative Colitis
Crohn's Disease

Study type

Observational

Funder types

Other

Identifiers

NCT03257345
RHM MED1307

Details and patient eligibility

About

Vedolizumab has been approved for the treatment of both ulcerative colitis and Crohn's disease. The aim of this study is to capture the early real life UK experience of vedolizumab including the outcomes of treatment, describing the patient population treated, drug persistence, IBD control PROM, durable remission, tolerance and safety.

Enrollment

360 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants being given vedolizumab as part of routine care, and vedo naïve prior to study
  • Age 18 or over
  • Written informed consent obtained from patient for participation in the UK IBD Registry

Exclusion criteria

  • Patient unwilling to take part in the UK IBD Registry
  • Unable to obtain written informed consent
  • Patient is, in the opinion of the investigator, not suitable to participate in the study
  • Patients with contraindications to the use of vedolizumab

Trial contacts and locations

22

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Central trial contact

Cheryl S Booker, BA; Fraser Cummings, MBChB

Data sourced from clinicaltrials.gov

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