Actively Recruiting
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
Eligibility Criteria
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
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
Complete this quick 3-step screening to check your eligibility
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
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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