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Timing is everything: early nausea relief in the ER

NCT ID NCT07523230

Symptom relief Sponsor: muzeyyen ataseven Source: ClinicalTrials.gov ↗

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at 200 adults in the emergency department who had nausea. It compared giving anti-nausea medicine within the first 30 minutes versus waiting longer. The goal was to see if earlier treatment reduces nausea more and makes patients more comfortable. Results could help ER doctors decide the best time to give nausea medication.

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

200 people

The number who actually took part.

Started

Feb 2026

Finished

Apr 2026

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

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

Inclusion Criteria: * Age ≥18 years * Presentation to the emergency department with nausea (with or without vomiting) * Receiving antiemetic treatment * Ability to communicate * Ability to provide informed consent * Ability to undergo nausea assessment using a Numeric Rating Scale (NRS) at initial evaluation Exclusion Criteria: * Altered level of consciousness (unconscious or confused) * Intubated patients * Severe psychiatric conditions (e.g., psychosis or delirium) * Patients in critical condition requiring immediate resuscitation * Hemodynamic instability * Inability to communicate (including language barrier or severe hearing/speech impairment preventing scale application) * Refusal to participate

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Conditions

The condition(s) this trial relates to.

Emergencies Nausea

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Emergency department patients Nausea

Contacts and locations

Locations

  • Istanbul Medipol University Hospital, Emergency Department

    Istanbul, 34810, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.