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Could a stick of gum soothe a spinning world?

NCT ID NCT07749573

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 06, 2026 · Last updated Aug 07, 2026 · Updated 1 time

Summary

This trial tests whether chewing sugar-free gum for 20 minutes, alongside standard intravenous medication, can reduce dizziness and nausea in adults with a common inner-ear condition called posterior canal BPPV. Participants are randomly assigned to either chew gum or receive standard treatment alone, with symptom severity measured before and after. The idea is that chewing may stimulate nerve pathways that help calm the vestibular system, potentially offering a simple, drug-free boost to standard care.

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 (sugar-free, mint-flavored) added to standard intravenous dimenhydrinate treatment
What this could lead to
If chewing gum helps, it could offer a simple, drug-free way to ease dizziness and nausea during BPPV attacks, potentially reducing reliance on sedating medications.
What could go wrong
This is a small, early-stage trial, and the effect may be modest or not clinically significant. Chewing gum might not work for everyone, and the study only measures short-term symptom changes.

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 88 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

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: * Aged 18-65 years * Duration of dizziness complaint less than 24 hours * Posterior canal BPPV diagnosis confirmed by the emergency physician via the Dix-Hallpike test * Intravenous administration of 50 mg dimenhydrinate in 100 cc 0.9% NaCl initiated by the responsible emergency physician * Symptomatic dizziness with VAS ≥ 4 * Alert, cooperative, and able to chew gum * Willingness to participate and provision of written informed consent Exclusion Criteria: * Findings suggestive of central vertigo (vertical nystagmus, diplopia, ataxia, hemiparesis, focal neurological deficit, etc.) * Pregnancy * Known gum intolerance, history of allergy to gum or its excipients, temporomandibular joint dysfunction, significant tooth loss, use of dentures or removable prosthetics that would prevent chewing * Altered level of consciousness * Central pathology detected on investigations performed during the visit * Hemodynamic and/or respiratory instability * Diagnosis other than posterior canal BPPV as the cause of vertigo * Treatment other than pharmacological therapy planned or already administered by the responsible emergency physician * Active vomiting at the time of enrollment * Severe dizziness with VAS ≥ 8 (excluded due to high likelihood of requiring additional treatment, risk of protocol deviation, and safety concerns regarding gum chewing) * Patients who initially consented but subsequently wish to withdraw from the study

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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

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  1. The places running it

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  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • Ankara Atatürk Sanatorium Training and Research Hospital

    Ankara, Turkey (Türkiye)

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