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Cool vapor may soothe Post-Surgery thirst and nausea

NCT ID NCT07273162

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether inhaling cool steam for 15 minutes can reduce shortness of breath, thirst, and nausea in 66 adults recovering from laparoscopic inguinal hernia surgery. Participants will be randomly assigned to receive cold vapor or standard care. Researchers will measure symptoms using simple scales and check vital signs like heart rate and oxygen levels.

What this could mean

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

Active substance
cold vapor inhalation
What this could lead to
If it works, this simple, drug-free method could help patients feel more comfortable after hernia surgery.
What could go wrong
This is a small, early-stage trial with only 66 people. The results may not apply to other surgeries or patients, and the effect may be small.

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 66 people

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

Expected to start

Dec 2025

An estimate. Start dates often move.

Expected to finish

Sep 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

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: * Volunteering to participate in the study * Being aged 18 years or older * Being able to speak and understand Turkish * Having cognitive, affective, and communicative competence * Having intact visual and auditory functions * Having undergone elective laparoscopic inguinal hernia surgery under general anesthesia * Having an ASA score of I or II * Having a total Modified Aldrete Score of ≥9 and a consciousness score of 2 (fully awake) in the postoperative period * Not having developed vomiting prior to the intervention * Having a body temperature within the normal physiological range (36-37.5 °C) Exclusion Criteria: * Having cold vapor application planned by physician order in the PACU prior to the study * Having signs and symptoms of upper or lower airway obstruction * Developing agitation and having communication insufficiency * Having an allergy to cold vapor application * Having a diagnosis of obstructive pulmonary disease (e.g., COPD, asthma) or heart failure * Having a known history of any neurological or psychiatric disease * Having a postoperative nasogastric catheter inserted * Having received preoperative diagnoses associated with nausea, vomiting, or dyspnea

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Conditions

The condition(s) this trial relates to.

Dyspnea Hernia, Inguinal Nausea

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

    1 site. 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

  • Erciyes University

    Kayseri, Kayseri, 38080, Turkey (Türkiye)