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Clinical Trials/NCT02316132
NCT02316132
Withdrawn
Not Applicable

Confocal Endomicroscopy for the Detection of Food Intolerances in Patients With IBS: Add on Control Group: Does Stress Cause Similar Mucosal Changes to Food Antigens?

University Hospital Schleswig-Holstein1 site in 1 countryStarted: December 2014Last updated:

Overview

Phase
Not Applicable
Status
Withdrawn
Sponsor
University Hospital Schleswig-Holstein
Locations
1
Primary Endpoint
visible marked increase of leaks/gaps with extrusion of fluorescein into the gut lumen.

Overview

Brief Summary

After standard endomicroscopy with fluorescein to investigate for dysplasia in Barrett's esophagus the endoscope will be forwarded into the 2nd part of the duodenum. Fluorescein is needed for CLE but is not part of the investigation.

Initial CLE baseline images will be taken to assure intact mucosa and allow later detailed baseline counts of intraepithelial lymphocytes (IEL) and epithelial breaks in the duodenal mucosa.

Thereafter, either 10 ml NaCl 0.9% or 100µg CRF topped up to 10ml with NaCL 0.9% (according to randomisation) will be injected intravenously. Endoscopist and assistant staff will be blinded to the randomisation. Subsequently, the gut surface will be examined for at least 5 min with endomicroscopy for any change in IEL, epithelial breaks/gaps with extrusion of fluorescein into the gut lumen and widening of intervillous space.

Post procedure mucosal fluid will be aspirated for assessment of mast cell tryptase and eosin catatonic protein (ECP), and 8 duodenal biopsies will be taken for 1) electron microscopy to visualise mast cell degranulation and 2) paraffin embedding for subsequent staining for mast cell tryptase to identify mast cell activation and numbers.

The procedure will take around 15 minutes in addition to the routine investigation performed prior to the study. A study outline is presented in figure 1.

Samples taken are the same amount as done in the previous food associated study.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age \>18 years
  • No abdominal symptoms such as bloating and abdominal pain
  • Barrett's esophagus
  • Independent indication for confocal laser endomicroscopy for evaluation of Barrett's dysplasia
  • Written informed consent for participation in this study

Exclusion Criteria

  • Any known other gastrointestinal disease including infection such as helicobacter pylori, Morbus Whipple or others, celiac disease, or chronic inflammatory bowel disease
  • Active or recent GI Bleeding
  • Stricture in the upper gastrointestinal tract
  • Impaired renal function (Creatinine \>1.2 mg/dL)
  • Pregnancy or breast feeding
  • Inability to obtain informed consent
  • Known allergy to Methylene blue or Fluorescein
  • Participation in other clinical trials within the last 4 weeks

Arms & Interventions

Stress

Active Comparator

Injection of corticotropin releasing factor

Intervention: Stress (Drug)

Control

Placebo Comparator

Injection of 0.9% saline 10 ml

Intervention: Control (Drug)

Outcomes

Primary Outcomes

visible marked increase of leaks/gaps with extrusion of fluorescein into the gut lumen.

Time Frame: immediate

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital Schleswig-Holstein
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mark Ellrichmann

Senior Consultant, Unit of Experimental Endoscopy

University Hospital Schleswig-Holstein

Study Sites (1)

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