Status:

COMPLETED

Identification of Predictive Factors of Postoperative Pain After Oral Surgery From Phenotypic Parameters Easily Accessible Preoperatively (PHEDOPO)

Lead Sponsor:

University Hospital, Clermont-Ferrand

Conditions:

Pain, Postoperative

Anxiety, Dental

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This project aims to study various predictive factors of postoperative pain after oral surgery among different parameters accessible preoperatively, in order to build a predictive model. It also aims ...

Detailed Description

This project aims to study various predictive factors of postoperative pain after oral surgery among different phenotypic parameters accessible to preoperative interrogation (anxiety about dental care...

Eligibility Criteria

Inclusion

  • Adult patient, male or female, eligible for dental extraction under local anesthesia,
  • either a tooth on the arch,
  • either wisdom tooth(s) (2 homolateral wisdom teeth (maxilla + mandibular) or a mandibular wisdom tooth).
  • Fluent in speaking and reading French.
  • Able to give informed consent to research.
  • Affiliation to a Social Security scheme.

Exclusion

  • Pregnant or breastfeeding women.
  • Contraindication to paracetamol, NSAIDs, tramadol, or anesthetic agents local.
  • Patient uncooperative, unlikely or unable to comply with all procedures of the protocol.
  • Chronic use of opiates, in a therapeutic or illicit context.
  • Chronic depression on long-term antidepressants.
  • Stomatological pathology that may interfere with the conduct of the intervention or modify the results: insufficient mouth opening, pathologies of the temporal mandibular joints ...
  • Active medical pathology, or any medical condition judged by the investigator to be incompatible with the study.
  • Patient under guardianship, curatorship or safeguard of justice.
  • Refusal to participate.

Key Trial Info

Start Date :

July 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 26 2024

Estimated Enrollment :

148 Patients enrolled

Trial Details

Trial ID

NCT05405088

Start Date

July 1 2022

End Date

June 26 2024

Last Update

November 12 2024

Active Locations (1)

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CHU de Clermont-Ferrand

Clermont-Ferrand, France, 63000