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

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Civil Hospices of Lyon

Status

Active, not recruiting

Conditions

Cardiac Surgery
Chronic Pain Post-Procedural
Sternotomy Closure,Open Heart Surgery

Treatments

Other: Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT06681272
2024-A01249-38 (Other Identifier)
69HCL24_0457

Details and patient eligibility

About

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.

Enrollment

84 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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 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 results of the present study.

Trial design

84 participants in 1 patient group

Adult patients undergoing scheduled sternotomy cardiac surgery
Description:
Cohort, cardiac surgery patients who develop chronic pain Chronic post-surgical pain is defined as pain localized to the surgical site, with no other attributable cause, that persists for more than three months after surgery and has an impact on quality of life.
Treatment:
Other: Questionnaire
Other: Questionnaire
Other: Questionnaire

Trial contacts and locations

1

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Central trial contact

Judit JORDANA BOFILL, PI-nurse; Matthias JACQUET-LAGREZE, Dr

Data sourced from clinicaltrials.gov

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