CClinicalTrials.gg
CompletedNCT04068350PEDIACHROUpdated Jun 18, 2026

Epidemiological Study of Post-operative Chronic Pediatric Pain.

An observational study in Chronic Pain and Postoperative Pain, sponsored by University Hospital, Bordeaux. Completed. Open to participants aged 6 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-06-18.

Sponsored by University Hospital, Bordeaux · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
582
Ages
6 Years to 18 Years
Sex
All
01

Study summary

This study aims to estimate prevalence and determine risk factors for chronic pain at 3 months post-operative in pediatric surgery.

Read the detailed description

Chronic pain, defined as continuous or intermittent pain for 3 months or more, postoperative because in the territory of the surgical procedure and does not exist before the operation, is common in adults. Its prevalence varies according to the surgeries between 10 and 50% of the operated adults. The factors potentially responsible for their occurrence are gradually being highlighted in the recent literature, which has made it possible to develop an appropriate analgesic management strategy.

In pediatric surgery, acute pain has long been known and treated as early as possible using multimodal analgesic techniques. On the other hand, there are very few studies evaluating postoperative chronic pain 3 months after infant surgery, as was the case a few years ago in adults.

This study aims to estimate prevalence and determine risk factors for chronic pain at 3 months post-operative in pediatric surgery.

02

Conditions studied

  • Chronic Pain
  • Postoperative Pain

Keywords

  • Pediatrics
03

In context

Chronic Pain

2,930 studies on the registry are indexed under Chronic Pain; 701 are open to participants now.

This study's enrollment of 582 is above the median of 126 across 688 observational studies indexed under Chronic Pain.

Browse Chronic Pain studies →

Lead sponsor

University Hospital, Bordeaux is the lead sponsor of 783 studies on the registry; 188 are open to participants now.

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

04

Who can participate

Ages eligible
6 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All children between the ages of 6 and 18, who are scheduled for surgery or video-surgery, scheduled or urgent, in the pediatric surgery department of the Bordeaux University Hospital. The main interventions concerned by this protocol are:

  • Thoracotomies and thoracoscopies
  • Cholécysctectomie
  • Laparotomy and appendectomy
  • Inguinal surgery (inguinal hernia and testicular ectopia)
  • Orthopedic surgery
  • Urologic surgery (hypospadias, circumcision and upper urinary tract surgery)

Inclusion criteria

All children between the ages of 6 and 18, who are scheduled for surgery or video-surgery, scheduled or urgent, in the pediatric surgery department of the Bordeaux University Hospital.

All patients who consented to participate in the research.

Exclusion criteria

Exclusion Criteria:

  • All children operated on outpatient surgery.
  • Children and parents with difficulties in understanding the questionnaires.
  • Refusal of the child or one of the parents.
  • Change of home planned during the post-operative follow-up period (3 months).
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
582 participants (actual)
Patient registry
No

Groups and cohorts

  • Single arm

    The evaluation at 3 months of the postoperative pain will be carried out without the information collected in preoperative and immediate postoperative.

    Other: Pain questionnaire

Interventions

  • OtherPain questionnaire

    Pain questionnaire, 3 months after surgery

06

What researchers measure

Primary outcomes

  1. Chronic postoperative pain

    Visual analogic scale from 0 to 100: (between 0 and 30: low pain, between 30 and 60: moderate pain, between 60 and 100: severe pain)

    Time frame: 3 months after surgery

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Picat MQ, Pellegrin I, Bitard J, Wittkop L, Proust-Lima C, Liquet B, Moreau JF, Bonnet F, Blanco P, Thiebaut R; ANRS CO3 Aquitaine Cohort. Integrative Analysis of Immunological Data to Explore Chronic Immune T-Cell Activation in Successfully Treated HIV Patients. PLoS One. 2017 Jan 3;12(1):e0169164. doi: 10.1371/journal.pone.0169164. eCollection 2017. PubMed 28046052 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04068350
Lead sponsor
University Hospital, Bordeaux
Responsible party
Sponsor
First posted
Aug 28, 2019
Start date
Mar 21, 2010
Primary completion
Dec 21, 2011
Completion
Dec 21, 2011
Last update
Jun 18, 2026

Study contacts

Hélène BATOZ, Dr
principal investigator · University Hospital, Bordeaux

Oversight

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

Not currently enrolling

This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion