Can a spoonful of slush beat water for Post-Surgery thirst?

NCT ID NCT07787416

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time

Summary

This trial tests four different methods—slush, stick ice, cold water spray, and routine care—to see which best relieves thirst-related discomfort after surgery. It includes 150 adults who had general anesthesia and feel thirsty. The study measures thirst intensity, comfort, and satisfaction to find the most effective approach.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Four methods to relieve thirst: slush, stick ice, cold water spray, and routine care
What this could lead to
If one method proves superior, it could become a standard, low-cost way to ease thirst and boost comfort for millions of post-surgery patients.
What could go wrong
This is a small, single-center trial, so results may not apply broadly. Also, the methods are compared for short-term relief, not long-term outcomes.

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

150 people

The number who actually took part.

Started

Nov 2022

Finished

Apr 2023

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 to 60 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: * Patients between the ages of 18-60 * General anesthesia for at least 1 hour * Absence of open wounds in the mouth and lips * Patients who can express their thirst verbally and score 4 or more on the numerical verbal scale * Patients who voluntarily agreed to participate in our study Exclusion Criteria: * Presence of pain, nausea and vomiting at the time of data collection * Those with DM and Chronic Kidney Failure * Patients who need intensive care after surgery * Those who have absolute oral intake restriction for more than 24 hours before and after surgery

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Conditions

The condition(s) this trial relates to.

Personal Satisfaction

As listed by the trial registrant

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

Contacts and locations

Locations

  • Afyonkarahisar Health Sciences University

    Afyonkarahisar, 03300, Turkey (Türkiye)

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