Evaluation of Pain Trajectories After Surgery and Their Potential Relationship With Chronicity at 3 Months (ETADOL)

Centre Hospitalier Universitaire de Nīmes

Status: Enrolling

Conditions: Surgical Procedures, Operative; Chronic Pain; Pain

Treatments: Other: In hospital pain evaluation; Other: In hospital questionnaires; Other: Telephone contact at 3 months

Study type: Observational

Funder types: Other

Identifiers

NCT05326737

2020-A03223-36 (Other Identifier)

LOCAL/2020/PC-02

Details and patient eligibility

About

The effective management of acute postoperative pain remains a daily challenge despite the organizational efforts made and the techniques put in place.

Thirty percent of patients who undergo surgery suffer from chronic post-surgical pain, of which 5 to 10% are of severe intensity. Many preoperative, intraoperative, and postoperative factors, related to the patient, the surgical procedure, or the anesthetic technique, have been incriminated as risk factors for chronic post-surgical pain. The severity of acute postoperative pain is recognized as one of the risk factors for the occurrence of chronic post-surgical pain on which we can hope to interact during the peri-operative period.

In this cohort study, we wish to define the typologies of postoperative pain trajectories observed from Day 0 to Day 7 and to estimate the proportion of patients with an abnormal resolution of pain in a model of organization such as that of our institution, in classic hospitalization and in ambulatory care.

Enrollment: 5,000 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• The patient must be insured or beneficiary of a health insurance plan
• The patient is available for 3 months of follow-up
• The patient has undergone a planned surgical procedure in one of the participating departments
• The patient is willing and able to respond to the study questionnaires

Exclusion criteria

• The patient is participating in another study
• The patient is in an exclusion period determined by a previous study
• The patient is under judicial protection, under tutorship or curatorship
• It is impossible to correctly inform the patient
• Patient admitted to the ICU and still intubated at day 1

Trial design

5,000 participants in 1 patient group

The study population

Description:

The study population consists of adult surgery patients at the Nîmes University Hospital, with recruitment based on the operating theater program and for a predefined list of surgeries.

Treatment:

Other: Telephone contact at 3 months

Other: In hospital questionnaires

Other: In hospital pain evaluation