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RecruitingNCT04608968Updated Nov 27, 2024

Pediatric Perioperative Satisfaction Questionnaire

An observational study in Perioperative, Children and Satisfaction, sponsored by University Hospital, Montpellier. Recruiting at 6 sites in France. Open to participants aged 7 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-27.

Sponsored by University Hospital, Montpellier · Observational

From the registry’s dates

  • Started Sep 2020; still recruiting 6 years 1 month later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
600
Ages
7 Years to 17 Years
Sex
All
01

Study summary

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

Read the detailed description

Step 1 : development of the questiontionnaire Face to face interview to report the satisfaction of the children after surgery and to identify recurrent themes to generate questions.

Step 2 : validation of the questionnaire Evaluation of the psychometric validity of the final questionnaire

02

Conditions studied

  • Perioperative
  • Children
  • Satisfaction

Keywords

  • Validity
  • Questionnaire
  • Children
  • health quality of life
  • Self report
03

In context

Lead sponsor

University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

children 7 years and older after surgery

Inclusion criteria

  • children 7 years and older
  • elective surgery
  • general anesthesia
  • abiliy to understand and read questions

Exclusion criteria

Exclusion criteria:

  • emergency
  • cognitive trouble
  • intellectual disability
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
600 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Children satisfaction after surgery

    to develop a questionnaire (score 0 to 100) to assess the satisfaction of children after surgery (from the day of surgery to 2 weeks)

    Time frame: at discharge of hospital ( from the day of surgery up 14 days)

Secondary outcomes

  1. postoperative pain intensity

    to assess the level of children postoperative pain intensity (from the day of surgery to 2 weeks). Pain was assessed using the Face Pain Scale revised tool (0-10).

    Time frame: at discharge of hospital ( from the day of surgery up 14 days)

  2. perioperative anxiety level

    to assess perioperative anxiety level using the Visual Analog Scale (0-10) of children after surgery (from the day of surgery to 2 weeks)

    Time frame: at discharge of hospital ( from the day of surgery up 14 days)

07

Study locations

6 of 6 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — NC

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 27, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04608968
Lead sponsor
University Hospital, Montpellier
Responsible party
Sponsor
First posted
Oct 30, 2020
Start date
Sep 1, 2020
Primary completion
Dec 1, 2026 (estimated)
Completion
Dec 1, 2026 (estimated)
Last update
Nov 27, 2024

Study contacts

sophie Bringuier
Contact
s-bringuierbranchereau@chu-montpellier.fr
04 67 33 86 61 ext. 33
Christophe DADURE, PhD
study director · University Hospital, Montpellier

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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