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Re-evaluation of anti-TNF use in a cohort of IBD patients in a non-academic hospital.

Withdrawn
Conditions
Inflammatory Bowel disease
10017969
Registration Number
NL-OMON38980
Lead Sponsor
Martini Ziekenhuis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

18 years or older
mentally compentent
diagnose of IBD
signed informed consent
well known history

Exclusion Criteria

pregnant women
existing treatment with MTX
history of fistels
second indication for anti TNF, such as Bechterew
serious co-morbidiy
unable to understand or write Dutch
serious transfusionreaction on infliximab or Humira in the past

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Which % of the studypopulation is succesfully changed into optimized thiopurine<br /><br>treatment? </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>1. Which subgroups are present?<br /><br>2. Which % and which subgroups can be succesfully changed into a optimized<br /><br>thiopurine treatment. (with TNF treatment)<br /><br>3. Which % and which subgroup can stop the anti-TNF long term (> one year)?</p><br>
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