The CalproSmartNOR Study - a New Clinical Tool for Monitoring Patients With Inflammatory Bowel Disease
Inflammatory Bowel Diseases
About this trial
This is an interventional diagnostic trial for Inflammatory Bowel Diseases focused on measuring Leukocyte L1 Antigen Complex, Feces, Cell Phone, Biomarkers, Recurrence, Prognosis, Clinical Chemistry Tests
Eligibility Criteria
Inclusion Criteria:
- Ulcerative colitis and Crohns disease diagnosis that fulfil the international Copenhagen diagnostic criteria for inflammatory bowel diseases (IBD)
- Remission, mild or moderate disease activity defined as 6-point Mayo Score <= 3 or Harvey Bradshaw index (HBI) <= 16
- Written and oral consent about participation in the project
- In a mental and physical state in which every step of the procedure is understood and feasible
- Ability to obtain and prepare a fecal sample and to use the Smartphone application (platforms such as Android or Iphone)
Exclusion Criteria:
- Severe disease activity defined as 6-point Mayo Score > 3 or HBI > 16
- Unable to read, understand or perform one or several steps of the procedure
Sites / Locations
- The Outpatient Clinic, Department of gastroenterology, Ålesund Hospital, Helse Møre og Romsdal HF
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
CalproSmart application
Standard follow-up
In addition to regular outpatient clinic visits and a routine CalproSmart test every 3 months, patients are instructed to obtain fecal samples if they experience symptoms suspect of recurrent IBD and to perform home analysis with CalproSmart™ system test kit
In addition to regular outpatient clinic visits and a routine calprotectin test in the same week as the visit date, patients bring home an Fecal-calprotectin tube and envelope and are instructed to obtain fecal samples and send these to local lab if they experience symptoms suspect of recurrent IBD