Please sign in to follow a disease.
Which reflux treatment works best? major trial to find out
NCT ID NCT07611162
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will compare five treatments for laryngopharyngeal reflux disease (LPRD) in 800 adults. Participants will receive either alginate, magaldrate, sucralfate, a proton pump inhibitor, or a special diet for three months. Researchers will measure symptom improvement to see which approach is most effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- alginate, magaldrate, sucralfate, proton pump inhibitors, and diet
- What this could lead to
- If successful, this study could identify which treatment works best for laryngopharyngeal reflux, helping doctors choose the most effective and tolerable option.
- What could go wrong
- This is a single trial with 800 participants, and results may not apply to everyone. The study hasn't started yet, so outcomes are uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 800 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
May 2026
An estimate. Start dates often move.
- Expected to finish
-
May 2030
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Positive 24-h HEMII-pH \> 1 event Exclusion Criteria: * Smoker (\>5 cigarettes/day) , alcohol dependence (\>3 units/day), * upper respiratory tract infection within the last month, * pregnancy, * neurological or psychiatric illness, * previous history of neck surgery or trauma, * malignancy, * history of head and neck radiotherapy * active seasonal allergies or asthma.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Laryngopharyngeal reflux disease are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
University of Mons
Mons, 7000, Belgium