Long-term Outcome of TNF Alpha Therapy in IBD

Sponsor
Medical University of Graz (Other)
Overall Status
Completed
CT.gov ID
NCT04575701
Collaborator
(none)
538
1
14
38.3

Study Details

Study Description

Brief Summary

The aim of this retrospective study is to assess the outcome of patients with inflammatory bowel disease (IBD) under TNF-alpha antibody therapy over a period of 20 years

Condition or Disease Intervention/Treatment Phase
  • Other: TNF Alpha therapy

Detailed Description

Long-term results published so far show that over the years a large part of patients have to stop TNF Alpha antibody therapy in IBD. Reasons are mostly loss of effectiveness or intolerance or side effects. Reasons for the termination are usually poorly characterized with regard to the exact reason and time. As a consequence, the aim of this retrospective study is to assess the outcome of patients with inflammatory bowel disease under TNF-alpha antibody therapy over a period of 20 years

Study Design

Study Type:
Observational
Actual Enrollment :
538 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Long-term Outcome of TNF Alpha Therapy in IBD
Actual Study Start Date :
May 1, 2019
Actual Primary Completion Date :
Jun 1, 2020
Actual Study Completion Date :
Jul 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Ulcerative Colitis (UC)

This Group includes all patients suffering from UC who have been treated with a TNF Alpha antibody within the last 20 years at the IBD outpatient clinic at our Hospital.

Other: TNF Alpha therapy
Retrospective analysis of outcome of first TNF Alpha therapy

Crohn's disease (CD)

This Group includes all patients suffering from CD who have been treated with a TNF Alpha antibody within the last 20 years at the IBD outpatient clinic at our Hospital.

Other: TNF Alpha therapy
Retrospective analysis of outcome of first TNF Alpha therapy

IBD unclassified

This Group includes all patients suffering from IBD unclassified who have been treated with a TNF Alpha antibody within the last 20 years at the IBD outpatient clinic at our Hospital.

Other: TNF Alpha therapy
Retrospective analysis of outcome of first TNF Alpha therapy

Outcome Measures

Primary Outcome Measures

  1. Length of first TNF Alpha Therapy in IBD patients [20 years]

    The main endpoint of this retrospective Analysis is the length of Treatment with the first TNF Alpha therapy in IBD

Secondary Outcome Measures

  1. Rate of further biologicals after first TNF Alpha therapy [20 years]

    Follow-up drug therapy after termination of TNF Alpha therapy

  2. Rate of surgical interventions after first TNF Alpha [20 years]

    Resections after the termination of first TNF Alpha therapy

  3. Reasons for discontinuing therapy [20 years]

    Loss of response, side effects etc.

  4. Predictive factors [20 years]

    Predictive factors for long-term response (BMI, CRP, Alb etc.)

  5. Number of side effects [20 years]

    Side effects of the primarily used TNF-alpha antibodies leading to discontinuation of the drug

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with a confirmed IBD diagnosis

  • TNF Alpha antibody therapy in the last 20 years at our outpatient clinic

Exclusion Criteria:
  • Not Meeting the inclusion criteria

  • Lack of clinical data, no follow up available

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Graz Graz Austria

Sponsors and Collaborators

  • Medical University of Graz

Investigators

  • Principal Investigator: Wolfgang Petritsch, Prof, Meduni Graz

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Medical University of Graz
ClinicalTrials.gov Identifier:
NCT04575701
Other Study ID Numbers:
  • 1465/2018
First Posted:
Oct 5, 2020
Last Update Posted:
Feb 25, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Feb 25, 2021