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Intercostal Cryoanalgesia for Chronic Pain After VATS Lung Resection (CRYO-VATS-2)

C

Centre hospitalier de l'Université de Montréal (CHUM)

Status

Active, not recruiting

Conditions

Surgery
Chronic Pain
Lung Cancer
Cryotherapy Effect

Treatments

Procedure: Single-injection paravertebral block
Procedure: Cryoanalgesia AND single-injection paravertebral block

Study type

Interventional

Funder types

Other

Identifiers

NCT05884099
2024-11564

Details and patient eligibility

About

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.

Full 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.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients scheduled for elective anatomical pulmonary resection (anatomical segmentectomy, lobectomy or bilobectomy) by VATS for lung cancer
  • American Society of Anesthesiologists (ASA) score 1-3

Exclusion criteria

  • Contraindication to the paravertebral block (coagulopathy, discontinuous paravertebral space, impossible thoracoscopic visualization of the paravertebral space)
  • Contraindication to intercostal cryoanalgesia (cold urticaria, cryoglobulinemia)
  • Epidural analgesia preferred (high risk of thoracotomy, marginal lung function)
  • Surgical criteria (conversion to thoracotomy, non anatomical wedge resection)
  • Preoperative thoracic or shoulder pain on the operated side
  • Known allergy to acetaminophen, celecoxib, sulfa, or both hydromorphone and morphine
  • History of thoracic surgery on the operated site
  • Regular use of opioids or medication with effects against neuropathic pain (tricyclics, gabapentinoids, duloxetine, venlafaxine)
  • Inability to understand pain scales or to communicate clearly despite adequate teaching
  • Contraindication to non-steroidal anti-inflammatory drugs (renal filtration rate < 60 mL/min, active gastric ulcer)
  • Pregnancy
  • Patient refusal to participate

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

80 participants in 2 patient groups

Intercostal cryoanalgesia AND single-injection paravertebral block
Experimental group
Description:
* Videothoracoscopic-guided single-injection paravertebral block at T5 with 0.4 mL/kg of Bupivacaine 0.5% with adrenalin 5 mcg/mL (maximum 40 mL) at the beginning of surgery * Cryoanalgesia 5 cm lateral to the neuraxial, on the inferior costal border, CO2 at (-)50C to (-)70C for 2 minutes, repeated on 7 costal levels (T3-T9), after the lung resection and before chest closure.
Treatment:
Procedure: Cryoanalgesia AND single-injection paravertebral block
Single-injection paravertebral block
Active Comparator group
Description:
-Videothoracoscopic-guided single-injection paravertebral block at T5 with 0.4 mL/kg of Bupivacaine 0.5% with adrenalin 5 mcg/mL (maximum 40 mL) at the beginning of surgery
Treatment:
Procedure: Single-injection paravertebral block

Trial contacts and locations

1

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Central trial contact

Alex Moore, MD; Evangelos Koliakos, MD

Data sourced from clinicaltrials.gov

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