Neuro-immune Interactions and PPI

NCT ID: NCT04713969

Last Updated: 2025-01-28

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-31
• Study Completion Date: 2024-09-23

Brief Summary

Prospective interventional study on duodenal neuro-immune interactions in healthy volunteers and functional dyspepsia patients and the effects of PPI

Detailed Description

Duodenal low-grade inflammation is frequently reported in functional dyspepsia (FD), while also neuronal and structural changes in duodenal submucosal ganglia have been described in FD patients. Proton pump inhibitors (PPI) are the first-line therapy in FD patients and are recently shown to have anti-inflammatory properties in FD. However, the exact mechanism of their anti-inflammatory action is unknow and their effect on duodenal nerve signalling remain unclear.

In this prospective interventional study, FD patients will undergo study procedures before and after treatment with pantoprazole (Pantomed®) 40mg twice daily during 4 weeks, with a baseline comparison to healthy volunteers.

This study aims to provide an in-deep characterization of the inflammatory infiltrate in the duodenum of FD patients, and to unravel the effect of PPI-therapy on neuronal signalling, duodenal inflammation and neuro-immune interactions in FD.

Novel insights in the pathophysiology of FD, including the duodenal mucosal inflammation and impaired neuronal functioning, can provide a better understanding of this commonly and costly disorder. Moreover, these results will help to elucidate the anti-inflammatory effect of PPI, which will contribute to the discovery of predictive markers for therapeutic efficacy of PPI in FD.

Conditions

Functional Dyspepsia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Functional dyspepsia patients before and after PPI

Pantoprazole 40mg twice daily in functional dyspepsia patients for 4 weeks

Group Type: EXPERIMENTAL

Pantoprazole 40mg

Intervention Type: DRUG

Pantoprazole 40mg twice daily

Healthy controls without PPI

Baseline investigations

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Pantoprazole 40mg

Pantoprazole 40mg twice daily

Intervention Type: DRUG

Other Intervention Names

Pantomed

Eligibility Criteria

Inclusion Criteria

• Patients with FD diagnosis as per Rome IV criteria (EPS or PDS).
• Normal investigation including upper GI endoscopy.
• Patients have confirmed duodenal mucosal eosinophilia.
• Patients witnessed written informed consent.
• Patients aged between 18 and 64 years inclusive.
• Male or female (not pregnant or lactating and using contraception or postmenopausal).
• Subjects are capable to understand the study and the questionnaires, and to comply with the study requirements.

Exclusion Criteria

• Patients with any condition which, in the opinion of the investigator, makes the patient unsuitable for entry into the study.
• Patients with any major psychiatric disorders (stable dose of single antidepressant allowed for psychiatric indication, no limitation for other indications).
• Patients presenting with predominant symptoms of irritable bowel syndrome (IBS) or of gastro-esophageal reflux disease (GERD).
• Patients with personal or family (first-degree relative) of diabetes mellitus, celiac disease, inflammatory bowel disease, psoriasis, lupus, scleroderma, rheumatic or other systemic auto-immune disease.
• Patients with eosinophilic esophagitis or eosinophilic gastroenteritis.
• Active H. pylori infection (or <6 months after eradication).
• Allergy or atopy, including therapy.
• Organic gastro-intestinal disease or history of gastrointestinal surgery other than appendectomy or splenectomy.
• Known impaired liver or kidney dysfunction, or coagulation disorders.
• Known HIV, HBV or HCV infection, including therapy.
• Active coronary or peripheral artery disease.
• Use of anti-inflammatory drugs or anti-allergy drugs <2 weeks before sampling.
• Use of immunosuppressants, antibiotics or acid-suppressive drugs <3 months before sampling.
• Use of prokinetics <2 weeks before sampling (unless if ≤3/week).
• Significant alcohol use (>10 units/week).
• Any use of alcohol or smoking <2 days before sampling.
• Active malignancy, including therapy.
• Females who are pregnant or lactating.
• Patients not capable to understand or be compliant with the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Universitaire Ziekenhuizen KU Leuven

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Tim Vanuytsel, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Universitaire Ziekenhuizen KU Leuven

Locations

KU Leuven

Leuven, Belgie, Belgium

Countries

Belgium

Other Identifiers

S64807/64847

Identifier Type: -

Identifier Source: org_study_id