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Recruiting NCT04608968

NCT04608968 Pediatric Perioperative Satisfaction Questionnaire

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Clinical Trial Summary
NCT ID NCT04608968
Status Recruiting
Phase
Sponsor University Hospital, Montpellier
Condition Perioperative
Study Type OBSERVATIONAL
Enrollment 600 participants
Start Date 2020-09-01
Primary Completion 2026-12-01

Eligibility & Interventions

Sex All sexes
Min Age 7 Years
Max Age 17 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 600 participants in total. It began in 2020-09-01 with a primary completion date of 2026-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim of this study is to develop and validate a self-report questionnaire to evalutate the satisfaction of the children after surgery.

Eligibility Criteria

Inclusion criteria: * children 7 years and older * elective surgery * general anesthesia * abiliy to understand and read questions Exclusion criteria: * emergency * cognitive trouble * intellectual disability

Contact & Investigator

Central Contact

sophie Bringuier

✉ s-bringuierbranchereau@chu-montpellier.fr

📞 04 67 33 86 61

Principal Investigator

Christophe DADURE, PhD

STUDY DIRECTOR

University Hospital, Montpellier

Frequently Asked Questions

Who can join the NCT04608968 clinical trial?

This trial is open to participants of all sexes, aged 7 Years or older, up to 17 Years, studying Perioperative. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04608968 currently recruiting?

Yes, NCT04608968 is actively recruiting participants. Contact the research team at s-bringuierbranchereau@chu-montpellier.fr for enrollment information.

Where is the NCT04608968 trial being conducted?

This trial is being conducted at Montpellier, France, Bordeaux, France, Grenoble, France, Nîmes, France and 2 additional locations.

Who is sponsoring the NCT04608968 clinical trial?

NCT04608968 is sponsored by University Hospital, Montpellier. The principal investigator is Christophe DADURE, PhD at University Hospital, Montpellier. The trial plans to enroll 600 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology