Preventive Skin Analgesia With Lidocaine Patch 5% for Controlling Post-thoracotomy Pain
Pain, Postoperative

About this trial
This is an interventional treatment trial for Pain, Postoperative focused on measuring Pre-emptive analgesia, Post-thoracotomy pain, Lidocaine patch
Eligibility Criteria
Inclusion Criteria:
- More than 18 years old
- Anatomical resection by standard lateral thoracotomy for treatment of non small cell lung cancer
Exclusion Criteria:
- Allergy to Lidocaine
- American Society of Anaesthesiologist (ASA) classification score more than 3
- History of previous thoracic surgical procedures and/or of chronic pain or taking regular analgesics
- Pneumonectomy or concomitant decortication and/or chest wall injury or resection,
- Psychiatric illness
- Participation to other studies
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Lidocaine Group
Placebo Patch
Lidocaine patch 5% (Lidoderm®, Endo Pharmaceuticals Inc, Malvern, PA, USA) measuring 10 x 14 cm and containing 700 mg of Lidocaine, was applied to cover the planned skin incision, marked with a pen by surgeon. Patch was applied for 12 hours during the night, removed for the subsequent 12 hours during the day, and then a new patch was applied at the same level the night after. This process was continued for 3 days before thoracotomy
A patch, that was identical in appearance to the active patch but did not contain Lidocaine, was applied to cover the planned skin incision, marked with a pen by surgeon. Patch was applied for 12 hours during the night, removed for the subsequent 12 hours during the day, and then a new patch was applied at the same level the night after. This process was continued for 3 days before thoracotomy