Clinical Trials Directory

Trials / Completed

CompletedNCT05884099

Intercostal Cryoanalgesia for Chronic Pain After VATS Lung Resection

Intercostal Cryoanalgesia for Prevention of Chronic Postoperative Pain Following Video-assisted Thoracoscopic Lung Cancer Resection

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM) · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Intercostal cryoanalgesia is a technique that allows extensive and prolonged analgesia of the hemithorax. The aim of this study is to demonstrate the efficacy of intercostal cryoanalgesia as an adjunct to a single-injection paravertebral block for the prevention of chronic thoracic pain after VATS lung resection surgery.

Detailed description

VATS lung resection is associated with a high incidence of persistent thoracic pain. To our knowledge, there is no study on the effect of cryoanalgesia on the incidence and severity of chronic thoracic pain 3 months after VATS lung resection. Intercostal cryoanalgesia is a technique that allows extensive and prolonged analgesia of the hemithorax. In a recent study by Ilfeld \& al, intercostal cryoanalgesia (combined with a single-injection paravertebral block) was able to drastically lower the incidence of chronic pain after total mastectomy compared to the use of the paravertebral block alone (3% vs 17%). The aim of this study is to demonstrate the efficacy of intercostal cryoanalgesia for the prevention of chronic thoracic pain after VATS lung resection surgery.

Conditions

Interventions

TypeNameDescription
PROCEDURECryoanalgesia AND single-injection paravertebral blockCO2 Cryoanalgesia AND paravertebral block with Bupivacaine 0.5%
PROCEDURESingle-injection paravertebral blockParavertebral block with Bupivacaine 0.5%

Timeline

Start date
2023-11-09
Primary completion
2025-01-21
Completion
2025-04-21
First posted
2023-06-01
Last updated
2025-07-04

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05884099. Inclusion in this directory is not an endorsement.