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Fructose Malabsorption in Northern Norway

Phase 2
Completed
Conditions
Fructose Malabsorption
Irritable Bowel Syndrome
Interventions
Behavioral: diet restriction
Registration Number
NCT00555191
Lead Sponsor
University Hospital of North Norway
Brief Summary

Different published studies has shown a possible co-variation between leakage of fructose to the great bowel and exacerbation of irritable bowel syndrome (IBS) symptoms.

The aim of the FINN trial is to study the role of fructose malabsorption in patients with IBS in order to evaluate different diagnostic criteria for fructose malabsorption and at the same time study the effect of diet treatment in this cohort of patients and estimate the prevalence of fructose malabsorption.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
182
Inclusion Criteria
  • IBS patients satisfying ROME 2 diagnostic criteria
Exclusion Criteria
  • Seriously ill
  • Organic abdominal disease
  • Other functional bowel disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1diet restrictionPATIENTS IN THIS ARM IS INSTRUCTED IN FRUCTOSE REDUCED DIET FOR A PERIOD OF 3 MONTHS
Primary Outcome Measures
NameTimeMethod
VAS score og specific abdominal complaints.SGA score of relief related to abdominal complaints.12 weeks
Secondary Outcome Measures
NameTimeMethod
Estimate sensitivity,specificity,negative and positive predictive value using 50 gm fructose in breath test.Validate questionary for intolerance.Validate VAS in judging changes in abdominal complaint.Examine polymorphism i Glut5 transporter gene.12 weeks

Trial Locations

Locations (1)

Hospital of Rana Medical Dep. Helgelandsykehuset HF

🇳🇴

Mo i Rana, Nordland, Norway

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