New study aims to take the fear out of needle sticks for kids
NCT ID NCT07410078
First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 2 times
Summary
This study compares three different oral premedication combinations in 135 children aged 4-12 who are scheduled for day surgery. The goal is to see which regimen helps children tolerate the IV insertion with less fear and distress. Researchers will measure anxiety, pain, and satisfaction from parents and doctors to find the best approach for a smoother experience.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 135 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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4 to 12 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pediatric patients aged 4-12 years * American Society of Anesthesiologists (ASA) physical status I-II * Scheduled for elective ambulatory (day-case) surgery * Eligible to receive oral premedication * Cognitive ability sufficient to complete behavioral and pain scale assessments * Written informed consent obtained from a parent or legal guardian Exclusion Criteria: * ASA physical status III or higher * Moderate to severe intellectual disability * Moderate to severe autism spectrum disorder * Known allergy or contraindication to midazolam, ketamine, or ibuprofen * History of sedative or opioid use within the previous 24 hours * Complete loss of premedication due to vomiting
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Conditions
The condition(s) this trial relates to.
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.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Ankara Etlik City Hospital
RECRUITINGAnkara, 06000, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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