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Rhomboid Intercostal Block Versus Retrolaminar Block for Postoperative Analgesia After Thoracoscopic Sympathectomy

Not Applicable
Recruiting
Conditions
Post Operative Pain
Registration Number
NCT06653803
Lead Sponsor
Damanhour Teaching Hospital
Brief Summary

Background: Although thoracoscopic sympathectomy is made via small incisions, it is associated with severe postoperative pain. Both Rhomboid intercostal block (RIB) and Retrolaminar block (RLB) are recent techniques used for pain control after such procedures

Objectives: To compare the effectiveness of RIB and RLB in providing postoperative analgesia after thoracoscopic sympathectomy in adult patients and their impact on the patient's outcomes.

Patients and Methods: This prospective, randomized (1:1), double-blind clinical trial; will be carried out on 60 patients scheduled for elective thoracoscopic sympathectomy under general anesthesia at our hospital. Patients will be randomly allocated into two equal groups (30 patients each) and will receive: in group A; general anesthesia with intraoperative ipsilateral ultrasound-guided RIB, whereas in group B; general anesthesia with intraoperative ipsilateral ultrasound-guided RLB.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • American Society of Anesthesiologists (ASA) physical status ≤ II
  • Age from 18 to 60 years
  • Body Mass Index (BMI) < 35 kg/m²
Exclusion Criteria
  • American Society of Anesthesiologists (ASA) physical status > II
  • Age < 18 years or > 60 years
  • Body Mass Index (BMI) ≥ 35
  • Local infection at the puncture site
  • Altered mental status
  • Pregnant women
  • Allergy to study drugs
  • Chronic pain
  • Coagulation abnormalities or on anticoagulants
  • Severe hepatic or kidney disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Mean and Standard deviation of time to the first request of postoperative rescue analgesic (minutes) (mean±SD)24 hours after the end of surgery

The time interval between the block performance and the first request of postoperative analgesia

Secondary Outcome Measures
NameTimeMethod
Mean and Standard deviation of Numeric Pain Rating Scale (NPRS) score (mean±SD)24 hours after the end of surgery

NPRS measures the severity of postoperative pain, it is a 11 point scale from 0-10; where 0=No pain and 10=Worst possible pain (At PACU, 1h, 3h, 6h, 12h, 18h, 24h) after the end of surgery

Mean and Standard deviation of the total dose of the rescue analgesic consumed (milligrams) (mean±SD)24 hours after the end of surgery

The total dose of the rescue analgesic consumed in the first 24 hours after the end of surgery

Trial Locations

Locations (1)

Damanhour Teaching Hospital

🇪🇬

Damanhūr, El-Beheira, Egypt

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