Small Intestinal Function in Patients With Cystic Fibrosis

Sponsor
University of Aarhus (Other)
Overall Status
Unknown status
CT.gov ID
NCT01468428
Collaborator
(none)
15
1
14
1.1

Study Details

Study Description

Brief Summary

In patients with Cystic fibrosis (CF) epithelial transport of chloride and sodium is disrupted in several organs such as airways, sweat glands, pancreas and intestines. Gastrointestinal symptoms are frequent but little is known about intestinal motility and function. Earlier studies using lactulose/hydrogen breath tests have found altered intestinal transit time. The method has several sources of errors and results have been questioned. This study is using a new, non invasive method to study intestinal motility patterns and transit times, Magnetic Tracking System - 1 (MTS-1).

The aim is to compare patterns of contractility and transit times in the stomach and small intestine in adult CF- patients with healthy controls.

Methods MTS-1 is performed without radiation and is associated with minimal discomfort for subjects. A small magnetic pill is ingest and detected by a matrix of sensors. Position and orientation of the magnet are defined by five coordinates (position: x, y, z, angle: φ, θ). Frequencies of slow waves as well as number and power of phase III contractions can be identified.

Colorectal transit times are determined with a plain abdominal x-ray. The subjects are asked to ingest a capsule containing 10 radiopaque markers on six consecutive days up to examination. The total number of markers in the entire colorectum is counted. Total transit time, as well as segmental is calculated.

Subjects 15 adult patients (> 18 years) with CF, homozygote for the mutation ΔF508, are studied. They are all pancreas insufficient (fecal elastase < 100 µg/g), with no previous intestinal resection or lung transplantation. None of them have diabetes. Patients are all in well-regulated pancreatic enzyme replacement therapy (PERT), thriving and with stabile weight over the last half year. They have had no treatment with antibiotics in the last 14 days up to the examination.

The hypothesis is that patterns of contractility and transit times are the same for CF-patients in well -regulated PERT as for healthy controls.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    15 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Small Intestinal Function in Patients With Cystic Fibrosis
    Study Start Date :
    Oct 1, 2010
    Anticipated Primary Completion Date :
    Dec 1, 2011
    Anticipated Study Completion Date :
    Dec 1, 2011

    Outcome Measures

    Primary Outcome Measures

    1. Small intestinal transit time []

      MTS-1: A small magnet pill is ingested and its movements are monitored and recorded from mouth to caecum. The transit time of the stomach and small intestine is determined by real-time recordings.

    Secondary Outcome Measures

    1. Colorectal transit time []

      Colorectal transit times are obtained using a plain abdominal x-ray after subjects has ingested 10 radiopaque markers on six consecutive days up to examination. The total number of markers in the entire colorectrum is counted and total as well as segmental transit times are calculated.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Cystic fibrosis, severe mutations

    • Pancreatic insufficiency(Fecal elastase < 100 µg/g)

    • Thriving, stabile weight over the last half year

    • No treatment with antibiotics in the last 14 days up to the examination

    Exclusion Criteria:
    • intestinal resection

    • lung transplantation

    • diabetes

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Faculty of Healthy Sciencies Aarhus Denmark

    Sponsors and Collaborators

    • University of Aarhus

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Aarhus
    ClinicalTrials.gov Identifier:
    NCT01468428
    Other Study ID Numbers:
    • UAarhus - VCF
    First Posted:
    Nov 9, 2011
    Last Update Posted:
    Nov 11, 2011
    Last Verified:
    Nov 1, 2011
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 11, 2011