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Clinical Trial Summary

Prospective, monocentric, observationnal study. The primary objective of this study is to identify if presurgical child or/and parental anxiety is predictive of chronic postsurgical pain in abdominal or urologic ambulatory surgery.


Clinical Trial Description

The post surgical pain guidelines recommend to identify predictive factors, especially for vulnerable subjects.

For children, there is few data about predictive factors of postoperative pain after ambulatory surgery.

The objective of this study is to collect preoperative data (preoperative children's anxiety and parental anxiety) and postoperative data (postoperative pain measure: the day of surgery and 3 months after surgery) for children undergoing abdominal ou urologic ambulatory surgery, and to determine if there is a relationship between these data (Odds Ratio) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04206956
Study type Observational
Source Centre Hospitalier de Saint-Brieuc
Contact Gwenaelle Le Garff, Dr
Phone +33296017277
Email gwenaelle.legarff@armorsante.bzh
Status Recruiting
Phase
Start date October 14, 2019
Completion date September 2020

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