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Rhomboid Intercostal and Subserratus Plane Block (RISS) for perioperative analgesia in patients undergoing thoracotomy; a prospective randomized controlled study

Not Applicable
Conditions
perioperative analgesia in patients undergoing open thoracotomy
Registration Number
PACTR202008534389448
Lead Sponsor
Faculty of Medicine Tanta University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

age 18 – 60 years
either gender
ASA I-III
undergoing elective open thoracotomy

Exclusion Criteria

patient refusal
allergy to the study drug
body mass index (BMI) > 35 kg/m2
any contraindication to regional anesthesia e.g. coagulopathy
pregnancy
drug or alcohol abuse
daily intake of opioid analgesics

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
VAS score during the first 24 h postoperatively
Secondary Outcome Measures
NameTimeMethod
intraoperative fentanyl consumption. ;the first 24 h postoperative cumulative morphine consumption;the time to first morphine dose
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