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Stavanger University Hospital Inflammatory Bowel Disease Trial

Recruiting
Conditions
IBD
Registration Number
NCT01551563
Lead Sponsor
Helse Stavanger HF
Brief Summary

The study aims at studying the outcomes of a protocol-based handling of newly diagnosed Inflammatory bowel disease ( IBD ) patients within a defined uptake area in Norway. It is a descriptive study and no hypothesis is predefined.

Cytokine studies, QoL and fatigue assessment will be included for hypothesis-generating purposes.

Detailed Description

none considered needed

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
700
Inclusion Criteria
  • newly diagnosed IBD
Exclusion Criteria
  • previous IBD with specific treatment within 10 year
  • inability to consent
  • inability to adhere to treatment protocol

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Clinical efficacy of IBD drug therapy5 years

Endoscopic, clinical and biochemical response

Secondary Outcome Measures
NameTimeMethod
Fatigue in patients with coeliac disease - substudy1 year

Fatigue severity and prevalence at diagnosis and after one year of gluten free diet

Fatigue in IBD5 years

Fatigue severity and prevalence at diagnosis and during follow-up

IBD and the intestinal microbiome5 years

Microbiome/eukaryome profiles associated with disease activity and treatment response from diagnosis and during follow-up

Trial Locations

Locations (1)

SUS

🇳🇴

Stavanger, Norway

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