About this trial
AimoftheWork To assess the efficiency of Opoid free anaesthesia with paravertebral block compared to opoid free anaesthesia with erector spinae plane block in patients undergoing Thoracotomy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients age between 18 and 70 .
Patients with ASAII and IIIstatus.
Patients undergoing open surgical Thoracotomy as in lobectomy, pneumonectomy, segmentectomy and decortication.
Gender both males and females.
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Group A :Thoracic paravertebral block
Procedure/SurgeryUltrasound guided thoracic paravertebral block performed at the T5 level using 20 ml of 0.5% bupivacaine for postoperative analgesia in patients undergoing lateral thoracotomy
Erector Spinae Plane Block
Procedure/Surgeryultrasound guided erector spinae plane block will be performed at the T5 level using 20 ml of 0.5% bupivacaine as part of an opoid sparing anesthesia protocol for lateral thoracotomy
Treatment groups
Trial outcomes
Primary outcomes
Total morphine consumption for the first 24 hours postoperative
Secondary outcomes
Postoperative pain
Postoperative pain will be assessed using vas score at 0,2,6,12,24 hours post operative
Sponsors and contacts
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