Dyspepsia Clinical Trial
Official title:
The Role of Mast Cells on Duodenal Permeability After Duodenal Acid Perfusion in Healthy Volunteers
This is a randomized, double-blind, cross-over study in healthy volunteers. In the first part, the duodenum of the participants will be perfused with acid or saline, during which intragastric pressure will be monitored to assess activation of the duodenogastric reflex. After perfusion, duodenal biopsies will be collected to evaluate mucosal integrity. In the second part, healthy volunteers are treated with the mast cell stabilizer disodium cromoglycate or with a placebo during 14 days. Subsequently, the duodenum will be perfused with acid and intragastric pressure and mucosal integrity will be evaluated.
Despite intensive research, the pathophysiology of functional dyspepsia remains unknown. The
investigators recently demonstrated that functional dyspepsia patients display impaired
duodenal mucosal integrity and low-grade mucosal inflammation. As studies have also shown
that functional dyspepsia patients present with an increased spontaneous duodenal acid
exposure, the hypothesis of this study is that increased duodenal acid exposure results in
increased duodenal permeability via mast cell activation. This will also induce activation
of the duodenogastric reflex, resulting in gastric relaxation, eventually leading to the
generation of dyspeptic symptoms. The general aim of this project is to assess the effect of
mast cell inhibition on duodenal mucosal integrity and intragastric pressure of healthy
volunteers after acid infusion in the duodenum.
The study will be a randomized, double-blind, cross-over study in 20 healthy volunteers and
consists of 2 parts. (1) In the first part, 10 healthy volunteers will be perfused with acid
(0.1N HCl) or 0.9% saline during 30 minutes at a rate of 5 mL/min with an interval of at
least one month. During acid/saline perfusion, intragastric pressure will be measured with a
high resolution manometry system to evaluate activation of the duodenogastric reflex.
Dyspeptic symptoms will be scored 1 minute before and every 5 minutes during the infusion.
After perfusion, endoscopy will be performed and duodenal biopsies will be obtained to
evaluate mucosal integrity using Ussing chambers and by assessing the expression of
cell-to-cell adhesion proteins (real-time PCR, immunofluorescence and western blot). (2) In
the second part, 10 healthy volunteers will be perfused with acid after a placebo treatment
and after treatment with the mast cell stabilizer disodium cromoglycate 100mg 4x2/day (with
an interval of at least one month). The rest of the study continues as described in part 1.
;
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06094062 -
Smartphone App-assisted PPI
|
N/A | |
Completed |
NCT03941288 -
Efficacy and Safety of Cannabidiol for Gastroparesis and Functional Dyspepsia
|
Phase 2 | |
Completed |
NCT04429802 -
The Effect of Prucalopride (Resolor®) on Gastric Motor Function and Gastric Sensitivity
|
N/A | |
Not yet recruiting |
NCT06369753 -
Visible Abdominal Distension
|
N/A | |
Withdrawn |
NCT02863822 -
Study to Evaluate Dietary Modification in Patients With Functional Dyspepsia.
|
N/A | |
Recruiting |
NCT00978159 -
Esomeprazole or Famotidine in the Management of Aspirin Related Non-Ulcer Dyspepsia
|
Phase 4 | |
Completed |
NCT00723502 -
Efficacy and Safety Study of Finafloxacin Used in Helicobacter Pylori Infected Patients
|
Phase 2 | |
Completed |
NCT00148603 -
Montelukast in the Treatment of Duodenal Eosinophilia
|
N/A | |
Completed |
NCT00217347 -
Evaluation of Efficiency of Esophageal Capsule Endoscopy in the Screening of Patients With Gastroesophageal Reflux Disease or Dyspepsia as Compared to Upper Endoscopy
|
N/A | |
Terminated |
NCT00220844 -
Tricyclic Antidepressants (TCAs) on Gastric Emptying
|
N/A | |
Completed |
NCT00232102 -
Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia
|
Phase 3 | |
Completed |
NCT00164996 -
Ultrathin Versus Conventional Esophagogastroduodenoscopy in Unsedated Patient With or Without Local Pharyngeal Anaesthesia
|
Phase 3 | |
Completed |
NCT00110968 -
Long-term Safety and Efficacy of Itopride Hydrochloride (HCl) in Patients Suffering From Functional Dyspepsia
|
Phase 3 | |
Completed |
NCT00232037 -
Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia
|
Phase 3 | |
Recruiting |
NCT05718960 -
Traditional Dietary Advice Versus Reassurance-alone in Postprandial Functional Dyspepsia
|
N/A | |
Completed |
NCT05750641 -
The Efficacy of Removal of Animal Milk From the Diet in Functional Dyspepsia: A Cross-sectional Study
|
||
Terminated |
NCT04247100 -
A Study of Randomized Sham-control Auricular TENS Unit Stimulation in Pediatric Functional Gastrointestinal Disorders
|
N/A | |
Completed |
NCT03252743 -
ICBT for Pain-predominant FGIDs in Children and Adolescents: an Implementation Study.
|
N/A | |
Completed |
NCT04697641 -
Helicobacter Pylori Eradication in Functional Dyspepsia
|
N/A | |
Recruiting |
NCT04918329 -
Functional Digestive Disorders Observatory
|