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Kids' Pre-Op anxiety linked to worse recovery, study finds

NCT ID NCT07343388

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 114 boys aged 2 to 7 having urogenital surgery to see if being anxious before the operation leads to more pain or confusion after waking up. Researchers measured anxiety before surgery and then tracked pain, delirium, and recovery speed in the recovery room. The goal is to understand if managing anxiety could improve surgical outcomes.

What this could mean

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

What this could lead to
If successful, this study could help doctors identify anxious children before surgery and tailor care to improve their recovery and reduce pain.
What could go wrong
This is a small observational study, so it can only show links, not cause and effect. Results may not apply to all children or surgeries.

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.

Participants

114 people

The number who actually took part.

Started

Jan 2026

Finished

Mar 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.

Who is studied

The study population consists of pediatric patients aged 2 to 7 years who are scheduled for elective urogenital surgical procedures at a tertiary pediatric training and research hospital. The cohort specifically focuses on patients undergoing common inguinoscrotal surgeries, including hypospadias repair, orchidopexy, and hydrocele surgery, under standardized general anesthesia. Participants are selected from patients who meet the ASA I-II physical status criteria and have no underlying neurological or psychiatric conditions that could interfere with anxiety and delirium assessments.

Ages

2 to 7 years

Sex

Male participants only

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: Male patients aged 2 to 7 years. ASA (American Society of Anesthesiologists) physical status I or II. Scheduled for elective urogenital surgery, specifically hypospadias repair, orchidopexy, or hydrocele surgery. Scheduled to undergo general anesthesia for the procedure. Patients with no history of neurological or psychiatric disorders. Provision of written informed consent by the parents or legal guardians. Exclusion Criteria: * Patients outside the specified age range (younger than 2 or older than 7 years). Female patients. Patients undergoing emergency surgeries or non-urogenital/non-inguinal procedures. Presence of a diagnosed cognitive impairment or developmental delay. Parental or legal guardian refusal to provide informed consent.

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Conditions

The condition(s) this trial relates to.

cryptorchidism hydrocele hypospadias Pain, Postoperative Postoperative Complications Urogenital Diseases

As listed by the trial registrant

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

Contacts and locations

Locations

  • Dr. Behcet Uz Children's Hospital

    Izmir, Konak, 35210, Turkey (Türkiye)

More trials for these conditions

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