Prevalence and Risk Factors for Chronic Post-Surgical Pain Following Video-Assisted Thoracic Surgery : The EVATHO Prospective Bicentric Cohort Study.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Montpellier

About this trial

Chronic post-surgical pain (CPSP) remains a common complication after thoracic surgery and may significantly impair patients' quality of life. Although the widespread adoption of video-assisted thoracic surgery (VATS) has reduced surgical trauma and improved postoperative recovery, a substantial proportion of patients still develop persistent pain.

The EVATHO study is a multicenter prospective observational cohort designed to determine the prevalence of CPSP three months after VATS and to identify perioperative factors associated with its development. Adult patients undergoing thoracic surgery by VATS at Montpellier and Nice University Hospitals will be prospectively enrolled.

Pain intensity, neuropathic pain characteristics, anxiety, depression, quality of life, and analgesic consumption will be assessed using validated questionnaires during the perioperative period and at 1 and 3 months after surgery. The results of this study may help identify patients at increased risk of CPSP and improve perioperative pain management strategies following thoracic surgery.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult patients undergoing video-assisted thoracic surgery (VATS) for thoracic surgery

Disqualifiers

Age <18 years

Adults under legal protection or unable to provide informed non-opposition

Patients unable to understand or complete the study questionnaires

Patients not affiliated with a French health insurance scheme.

Trial population

Adult patients undergoing video-assisted thoracic surgery (VATS) for pulmonary resection, pleural procedures, chest wall surgery, or lung biopsy at Montpellier and Nice University Hospitals.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Number of participants with chronic post-surgical pain

Chronic post-surgical pain defined as a Brief Pain Inventory (BPI) average pain score greater than 3 at the 3-month postoperative follow-up.

Time frame
3 months after surgery.

Secondary outcomes

1

Postoperative pain at 1 month after VATS

Post-surgical pain defined as a Brief Pain Inventory (BPI) average pain score greater than 3 at the 1-month postoperative follow-up.

Time frame
1 month after thoracic surgery
2

Visual Analogue Scale (VAS) pain score

Pain intensity measured using the Visual Analogue Scale (VAS), with scores ranging from 0 (no pain) to 10 (worst imaginable pain).

Time frame
Preoperative assessment, postoperative day 1, postoperative day 2, 1 month, and 3 months after surgery.
3

Cumulative postoperative opioid consumption.

Total opioid consumption during the postoperative period as morphine milligram equivalents

Time frame
Postoperative day 1, postoperative day 2, 1 month, and 3 months after surgery.
4

Douleur Neuropathie 4 (DN4) score

Neuropathic pain measured using the Douleur Neuropathique 4 (DN4) questionnaire. Scores range from 0 to 10, with scores greater than or equal to 4 indicating neuropathic pain.

Time frame
Preoperative assessment, postoperative day 1, postoperative day 2, 1 month, and 3 months after surgery.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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