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Coconut oil vs. glycerol: a mouth care showdown for seniors

NCT ID NCT07406425

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares coconut oil mouth care to standard glycerol sticks for elderly patients in geriatric hospitals who cannot clean their own mouths. Researchers will check if coconut oil improves oral health scores over 8 days. The goal is to find a better way to keep mouths healthy in older adults.

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

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

About 94 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

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

75 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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients aged 75 and over * Patients hospitalised in geriatric medicine and geriatric SMR departments * Patients able to open their mouths for treatment * Patients not able to carry out their oral hygiene on their own * Patients who have given their written consent (consent of the patient or patient consent accompanied by the designated representative if the patient is unable to give written consent) Exclusion Criteria: * Patients with a known allergy to coconut * Patients requiring medicated mouth care as prescribed by a doctor * Patients under guardianship, tutorship or curatorship * Confused patients who have had medically diagnosed dehydration for less than 48 hours * Patients with swallowing difficulties * Patients in the terminal phase of end of life Secondary exclusion criteria: * Patients leaving the department between D1 and D8 (whatever the reason for discharge, and including in the event of death) * Patients whose condition progresses towards a terminal phase of the end of life between D1 and D8 * Patients experiencing an allergic reaction to Coconut Oil during the study * Patients who may present with dehydration during the study

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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.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • CH de Brive

    Brive-la-Gaillarde, 19100, France

  • CHU Limoges

    Limoges, 87042, France

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