Post Operative Pain
Conditions
Brief summary
This double-blinded, randomized controlled study was done on 60 patients older than 18 years undergoing thoracotomy. Patients were allocated into two equal groups (30 patients each). Group S: Standard anesthesia in addition to SPB. II. Group P: Standard anesthesia in addition to PVB.
Interventions
a US-guided SPB was performed after induction of general anesthesia with the patient lying supine.
Standard anesthesia in addition to para-vertebral block
Sponsors
Study design
Eligibility
Inclusion criteria
* patients more than 18 ys undergoing thoracotomy operation
Exclusion criteria
* morbid obesity (Body mass index \> 40) * impossibility of anatomical structures US identification in a satisfactory way * opioids treatment before surgery or substance abuse, * sepsis and/or infection at the puncture sites
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| prevention of post-operative pain | 72 hours | reduction of visual analogue score |
| reduction of analgesic requirement | 72 hours | — |
Countries
Egypt