Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06984484

Performance and Safety of Afluxin® in Patients With Gastroesophageal Reflux Disease

Led by Devintec Sagl · Updated on 2026-04-08

208

Participants Needed

7

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Gastroesophageal Reflux Disease (GERD) is a chronic condition in which stomach acid flows back into the esophagus, causing irritation and inflammation. GERD is categorized into Nonerosive Reflux Disease (NERD), Erosive Esophagitis (EE), and Barrett's esophagus (BE). Common symptoms include heartburn and acid regurgitation. Lifestyle factors such as smoking, obesity, and Helicobacter pylori infection can increase the risk of developing GERD. The clinical management of GERD typically involves Proton Pump Inhibitors (PPIs) therapy, which, although effective, may not benefit all patients and can be associated with long-term risks. The American College of Gastroenterology (ACG) suggests PPIs discontinuation or on-demand therapy for uncomplicated GERD after an 8-week trial. However, evidence indicates that PPIs are used more frequently, often long-term and in high doses, and not necessarily according to recommendations. Moreover, the availability of Over-The-Counter (OTC) PPIs has led to prolonged use by patients without medical guidance. Concerns have been raised due to potential side effects of long-term PPIs use, including enteric, respiratory, and urinary tract infections, as well as an increased risk of vitamin and mineral deficiencies and osteoporosis. Alternatives to PPIs include Histamine-2 Receptor Antagonists (H2RAs), antacids and alginate-based formulations. Among OTC treatments, medical devices formulated with natural components are also gaining attention for their potential performance and tolerability in managing mild to moderate GERD symptoms. These alternatives could address the unmet needs of NERD patients, especially those with a low response to PPIs treatment and provide an option without the potential side effects of prolonged PPIs use. Afluxin® is a class III medical device, containing functional substances (tamarind seed polysaccharide, pea protein and polyacrylic acid), formulated for the treatment of mild to moderate GERD. Preclinical data have shown that Afluxin® is able to create a protective barrier over the gastroesophageal epithelium, preventing reflux damage. In vitro studies suggest that Afluxin® effectively binds to the esophageal and gastric mucosa, reducing abnormal permeability caused by acid reflux. Moreover, in vivo evidence shows that Afluxin® can increase gastric pH, reduce epigastric pain, esophageal damage, and inflammatory markers associated with GERD. Given the encouraging results obtained in preclinical investigations, this study is designed to provide clinical evidence to support the performance and safety of Afluxin® in reducing gastrointestinal symptoms of patients with mild to moderate GERD in a multicenter, randomized, double-blind, parallel-group, Afluxin® stick pack vs. inactive control clinical investigation.

CONDITIONS

Official Title

Performance and Safety of Afluxin® in Patients With Gastroesophageal Reflux Disease

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female patients aged 18 to 75 years
  • Ongoing heartburn and/or acid regurgitation symptoms of at least mild to moderate severity during the 7 days before treatment
  • No use of proton pump inhibitors, histamine-2 receptor antagonists, antacids, alginates, or similar medical devices in the last week before screening
  • Provided written informed consent and understand study procedures
  • Females of childbearing potential must have a negative pregnancy test and use effective contraception throughout the study
Not Eligible

You will not qualify if you...

  • Allergy to any components of Afluxin or placebo
  • Presence of rhinosinusitis or bronchitis
  • History or signs of other gastrointestinal diseases such as erosive GERD, Barrett's esophagus, peptic ulcers, hiatus hernia over 3 cm, Zollinger-Ellison syndrome, esophageal or gastric cancer, pyloric stenosis, previous gastrointestinal surgery, intestinal obstruction, pernicious anemia, H. pylori eradication need, or recent gastrointestinal bleeding
  • Diagnosis of functional dyspepsia with postprandial distress syndrome
  • History of gastro-esophageal surgery or bariatric procedures
  • Any active malignancy except non-invasive skin cancers
  • Use of prokinetics, systemic steroids, or NSAIDs in the last week before screening
  • Pregnant or lactating women
  • Participation in other clinical trials within 30 days before screening
  • Clinically significant or unstable diseases that could interfere with study participation as judged by the investigator

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 7 locations

1

IRCCS Policlinico San Martino

Genova, Italy, 16132

Actively Recruiting

2

IRCCS Ca' Granda Ospedale Maggiore Policlinico Foundation

Milan, Italy, 20122

Actively Recruiting

3

AOU Federico II di Napoli

Naples, Italy, 80131

Actively Recruiting

4

Azienda Ospedale Università Padova

Padova, Italy, 35128

Actively Recruiting

5

S. Andrea Ospedale Universitario

Roma, Italy, 00189

Actively Recruiting

6

Humanitas Research Hospital

Rozzano (MI), Italy, 20089

Actively Recruiting

7

A.O.U. Città della Salute e della Scienza di Torino

Torino, Italy, 10126

Actively Recruiting

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Research Team

D

Daniela Salvati

CONTACT

M

Maria Dini

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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