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NCT Number: NCT05681572

Effect of Sedative and Anxiolytic Premedication on Children Experience After General Anesthesia

Children undergoing general anesthesia for surgery commonly need sedative and anxiolytic premedication but little clinical evidence supports is benefit for children older than 7 years old.

The aim of this prospective randomized clinical trial is to assess the impact of pharmacologic premedication on perioperative children experience.

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Key information

Age range

7 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Uhmontpellier

Montpellier, 34295, France

Location status: Recruiting

Location contact

Sophie BRINGUIER, PHARM D, phD

CONTACT

[email protected]

0467338661 ext. +33

About this study

Surgery is a stressful experience in children with preoperative and postoperative anxiety.

For preschooler undergoing surgery, anxiety is the highest in the preoperative period.

Most of studies have been conducted on young children (< 7yrs old) to show the relationship between preoperative anxiety and emergence of delirium and postoperative maladaptive behavioral changes.

Sedative and anxiolytic medication is frequently used in children to reduce anxiety and postoperative maladaptive experiences. Nevertheless, little clinical evidence supports is benefit for children older than 7 years.

Treating anxiety is not necessarily associated with better experience in all children because premedication causes postoperative sedation, amnesia and cognitive impairment.

The aim of this prospective randomized clinical trial is to assess the impact of pharmacologic premedication on perioperative children experience using self-report questionnaire.

Patients are randomized to 2 groups to received pharmacologic premedication or placebo.

For the premedication group, children are randomly allocated to be premedicated with either with the midazolam or dexmedetomidine

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject over 7 and under 18 years of age
  • Subjects who are scheduled for surgery
  • Subject who will be under general anesthesia
  • Subject able to complete a self-questionnaire in French

Exclusion criteria

  • Subject who has already participated in the pediaPREM study
  • Subject with a treated anxiety disorder
  • Subject with cognitive disorders
  • Subject suffering from chronic pain (outside the operated area)
  • Subject with ADD (Attention Deficit Disorder) with or without hyperactivity, with or without treatment
  • Subject suffering from mental retardation
  • Subjects receiving psychotropic treatment
  • Subject whose intervention could reduce the ability to complete a self-questionnaire (neurosurgery etc.)
  • Subject with a contra-indication to midazolam and its excipients
  • Subject with a contra-indication to dexmedetomidine and its excipients
  • Subjects who need to receive intravenous alpha agonist in perioperative
  • Subjects requiring emergency intervention
  • Subjects requiring preoperative hypnosis
  • Subject who needs general anesthesia for diagnostic purposes (biopsy, etc...)
  • Subject having had a surgical intervention in the month preceding the inclusion.
  • Subject who will have an iterative surgical intervention within 15 days (removal of material, burns etc...)
  • Subjects who are scheduled for surgery as part of oncology management
  • Pregnant or breastfeeding woman
  • Subject whose two parents have not signed a written informed consent
  • Subjects who are not affiliated with or benefiting from a social security plan

Treatment and study plan

midazolam

Drug

45 minutes before entering the operating room, patient receives the oral treatment according to their randomization arm, here Midazolam , by a blinded nurse.

Dexmedetomidine

Drug

45 minutes before entering the operating room, patient receives the oral treatment according to their randomization arm, here Dexmedetomidine , by a blinded nurse.

Placebo

Drug

45 minutes before entering the operating room, patient receives the oral treatment according to their randomization arm, here Grenadine Syrup, by a blinded nurse.

Primary outcomes

  1. EVANpedia Score

    Time frame: from the day of surgery up to the day one after surgery

    To evaluate patient experience of the perioperative and post-operative period

Secondary outcomes

  1. VAS-anxiety Scores

    Time frame: from preoperative period up to 6 postoperative month

    To evaluate the perioperative level of anxiety thanks to the Visual Analogue Scale (VAS)

  2. Postoperative waking delay

    Time frame: from the end of the surgery up to the exit of the recovery room

    Time to wake up after surgery (minutes) to evaluate the delay emergence from anesthesia

  3. Modified Brice questionnaire Score

    Time frame: from the day of surgery up to 1 day

    To evaluate postoperative amnesia after anesthesia

  4. Post Hospitalization Behavior Scores

    Time frame: 15 postoperative days

    To evaluate changes of behavioral (appetite, sleep, sociability) after surgery

  5. quality of life

    Time frame: 6 postoperative months

    to evaluate the impact of the perioperative experience on the long-term experience

  6. neuropathic pain

    Time frame: 6 postoperative month

    to evaluate the percentage of patients with long-term neuropathic pain

  7. FPS-r scores

    Time frame: from the end of the surgery up to 6 post-operative month

    To evaluate the Postoperative level of pain thanks to the Faces Pain Scale-revised (FPS-r)

  8. Quality of life PedsQL

    Time frame: Up to 6 months post-operatively

    The quality of life will be measured by PedsQL in order to evaluate the impact of the perioperative experience on the long-term experience. The 23 questions cover 4 different domains: physical functioning (8 items), emotional functioning (5 items), social functioning (5 items) and academic functioning (5 items).

    The parent questionnaire assesses parents' perceptions of their child's health-related quality of life. On the PedsQL Generic Core Scales, for ease of interpretability, items are reversed scored and linearly transformed to a 0-100 scale, so that higher scores indicate better HRQOL (Health-Related Quality of Life).

Study contacts

Contact information is provided by the study sponsor or research team.

Sophie BRINGUIER, PHD

CONTACT

[email protected]

0467338661 ext. +33

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Registry information

Official study title

" Effect of Sedative and Anxiolytic Premedication on Children Experience After General Anesthesia " The pediaPREM Study.

Acronym: pediaPREM

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Jan 12, 2023
Registry last updated
Jul 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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