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Clinical Trials/NCT04068350
NCT04068350
Completed
N/A

Epidemiological Study of Post-operative Chronic Pediatric Pain.

University Hospital, Bordeaux0 sites582 target enrollmentMarch 21, 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
University Hospital, Bordeaux
Enrollment
582
Primary Endpoint
Chronic postoperative pain
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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

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.

Registry
clinicaltrials.gov
Start Date
March 21, 2010
End Date
December 21, 2011
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Bordeaux
Responsible Party
Sponsor

Eligibility Criteria

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).

Outcomes

Primary Outcomes

Chronic postoperative pain

Time Frame: 3 months after surgery

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)

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