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Quick Pre-Surgery therapy eases anxiety and pain for kidney donors

NCT ID NCT07261917

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested whether a brief psychiatric session one hour before surgery could help living kidney donors feel less anxious, have more stable vital signs during surgery, and experience less pain afterward. 123 donors took part, with some receiving the therapy and others standard care. The goal was to see if this simple, low-cost support could improve the donor's experience and recovery.

What this could mean

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

Active substance
Preoperative psychiatric consultation (psychoeducation, breathing exercises, guided imagery)
What this could lead to
If effective, this approach could become a standard, low-cost way to help kidney donors feel calmer and recover with less pain.
What could go wrong
This is a small, completed study without a later phase. The intervention is brief and may not work for everyone or in different hospital settings.

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

123 people

The number who actually took part.

Started

Nov 2023

Finished

Nov 2024

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

Accepted

You do not need to have the condition being studied to take part.

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 or older * American Society of Anesthesiologists (ASA) physical status Class I-II * Voluntary participation in the study Exclusion Criteria: * Diagnosed diabetes mellitus (DM) * Development of postoperative delirium * Previously diagnosed psychiatric disorder or current use of psychiatric medications * History of analgesic drug use within the last one month * Diagnosed neurological disorder * Diagnosed musculoskeletal disorder * Chronic pain or receiving chronic pain treatment * Recent severe psychological trauma or relevant psychosocial stressors

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Contacts and locations

Locations

  • Akdeniz University Hospital

    Antalya, Antalya, 07000, Turkey (Türkiye)

More trials for these conditions

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