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Epidemiological Study of Post-operative Chronic Pediatric Pain. (PEDIACHRO)

U

University Hospital of Bordeaux

Status

Completed

Conditions

Postoperative Pain
Chronic Pain

Treatments

Other: Pain questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT04068350
CHUBX 2009/18

Details and patient eligibility

About

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

Full 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.

Enrollment

582 patients

Sex

All

Ages

6 to 18 years old

Volunteers

No Healthy Volunteers

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

  • 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).

Trial design

582 participants in 1 patient group

Single arm
Description:
The evaluation at 3 months of the postoperative pain will be carried out without the information collected in preoperative and immediate postoperative.
Treatment:
Other: Pain questionnaire

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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