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Efficacy Assessment and Monitoring of Subcutaneous Infliximab Levels.

F

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Status

Completed

Conditions

Inflammatory Bowel Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT05071404
FIS-INF-2020-01

Details and patient eligibility

About

Retrospective observational study in which the efficacy of infliximab is studied in patients with inflammatory bowel disease and its subcutaneous levels are monitored.

Full description

Retrospective observational study in which the efficacy of infliximab is studied in patients with inflammatory bowel disease and its subcutaneous levels are monitored.

Treatment is prior to and independent of the patient's participation in the study and is governed by clinical judgment criteria and routine clinical practice, not performing any diagnostic or follow-up intervention that is not routine clinical practice.

Patients are older than 14 years who suffer from inflammatory bowel disease and who receive remsima as routine treatment.

The source of information will be the patient's medical history.

Enrollment

17 patients

Sex

All

Ages

14+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with inflammatory bowel disease.
  • Over 14 years old.
  • Receive Remsin as a treatment for his disease. And always this treatment that the patient is going to receive is governed by the criteria of clinical judgment and routine clinical practice, not performing any diagnostic or follow-up intervention that is not routine clinical practice.

Exclusion criteria

  • Patients with inflammatory bowel disease under 14 years of age.
  • Or older than this age with inflammatory bowel disease who do not attend the established check-ups

Trial design

17 participants in 1 patient group

Cases
Description:
Patients treated with infliximab sc.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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