Prediction of Chronic Pain in Cardiac Surgery: Evaluation by Algocartography Predict-ALGOCARTE

Last updated: March 11, 2026
Sponsor: Hospices Civils de Lyon
Overall Status: Completed

Phase

N/A

Condition

Cardiac Surgery

Pain

Chronic Pain

Treatment

Questionnaire

Clinical Study ID

NCT06681272
69HCL24_0457
2024-A01249-38
  • Ages > 18
  • All Genders

Study Summary

Sternotomy results in chronic postoperative pain in 30-55% of subjects. Few studies have been published on chronic pain in cardiac surgery, but there appears to be a relationship between the area of peri-scar hyperalgesia, which is indicative of postoperative hyperalgesia, and the occurrence of persistent pain 6 months after surgery. The aim of this study was therefore to assess whether the area of the postoperative hyperalgesia zone predicts chronic pain at 3 months post-surgery in cardiac surgery. To define the area of hyperalgesia at Day 2, pain mapping (algocartography) will be performed in patients who have had a sternotomy in cardiac surgery, together with pain assessment using the Simple Digital Pain Scale. Von Frey filaments of different sizes will be used for mapping. At Day 90, additional quality-of-life questionnaires will be carried out to check whether chronic pain is still present. A simple numerical scale (ENS) assessment at rest and during activity, and a record of pain-relieving treatments related to the surgery will also be carried out during this call.

The investigators hypothesize that the area of the zone of hyperalgesia assessed at Day 2 predicts the occurrence of chronic pain at 3 months.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Scheduled surgery

  • Conventional cardiac surgery by sternotomy: valve repair or replacement, coronary,thoracic aortic or combined surgery

  • Age over 18

  • No opposition from patient

  • Patient affiliated to a social security

Exclusion

Exclusion Criteria:

  • Emergency surgery

  • Patient refusal

  • Redux surgery

  • Patients under guardianship

  • History of drug addiction

  • Preoperative opioid treatment

  • Morbid obesity (body mass index >30kg/m2)

  • Pregnant or breast-feeding women

  • Patients taking part in another clinical study likely to interfere with the resultsof the present study.

Study Design

Total Participants: 84
Treatment Group(s): 1
Primary Treatment: Questionnaire
Phase:
Study Start date:
November 27, 2024
Estimated Completion Date:
February 27, 2026

Connect with a study center

  • Service Anesthésie réanimation Hôpital Louis Pradel, Groupement Hospitalier Est Adresse 28 av. de Doyen Lépine 69677 BRON Cedex

    Bron, France 69677
    France

    Site Not Available

  • Service Anesthésie réanimation Hôpital Louis Pradel, Groupement Hospitalier Est Adresse 28 av. de Doyen Lépine 69677 BRON Cedex

    Bron 3029931, France 69677
    France

    Site Not Available

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