Chewing gum tested as surprising remedy for medication side effect
NCT ID NCT07158359
First seen Jun 24, 2026 · Last updated Jun 26, 2026 · Updated 2 times
Summary
This study tests whether chewing gum can reduce excessive drooling caused by psychiatric medications. Researchers will compare 46 adults who chew gum as part of a swallowing program to those who don't. The goal is to find a simple, non-drug solution for this uncomfortable side effect.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- chewing gum
- What this could lead to
- If it works, this could offer a simple, drug-free way to manage drooling caused by psychiatric medications.
- What could go wrong
- This is a small pilot study with only 46 people, so results may not apply widely. Chewing gum might not reduce saliva enough to make a real difference.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 46 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2025
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Adults aged 18 to 65 years. * Hospitalized at Cadillac Hospital, either in full inpatient care or at the rehabilitation facility, excluding the UHSA. * Experiencing iatrogenic hypersalivation induced by psychotropic medications. * Salivary flow causing functional impairment for the patient, or observed by family members or healthcare providers. * With or without pharmacological management of hypersalivation. * Individuals under legal protective measures may be included. * Provided written informed consent prior to participation. Exclusion Criteria: * Anatomical/morphological anomaly affecting mastication/swallowing * Swallowing disorder of organic etiology (e.g., neurological deficit due to stroke, neurodegenerative disease, oropharyngeal surgery, etc.) * Known risk of aspiration with liquids * Patient refusal of chewing gum or inability to obtain consent (e.g., non-communicative patients) * Oral/dental condition preventing mastication
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Conditions
The condition(s) this trial relates to.
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.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
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