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SAPB with Mg and Buprenorphine for Postoperative Pain
N/A
Waitlist Available
Research Sponsored by Wayne State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
- Patients undergoing video-assisted thoracoscopy
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights
Study Summary
This trial will test whether adding the serratus anterior plane block (SAPB) to standard pain relief can improve postoperative pain for patients undergoing video-assisted thoracoscopic surgery.
Eligible Conditions
- Postoperative Pain
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Post-operative total opioid consumption (oral morphine equivalents)
Visual analog scale (VAS) pain scores
Secondary outcome measures
Acetaminophen consumption
Nausea
NSAID (ketorolac) consumption
Trial Design
3Treatment groups
Active Control
Group I: SAPB with Mg and BuprenorphineActive Control1 Intervention
40 Patients - Patients will receive 30 mL of 0.25% bupivacaine with 150 mg of Mg and 300 mcg of buprenorphine injected below the serratus anterior muscle in the caudal direction using ultrasound guidance.
Group II: SAPBActive Control1 Intervention
40 Patients - Patients will receive 30 mL of 0.25% bupivacaine injected below the serratus anterior muscle in the caudal direction using ultrasound guidance.
Group III: SAPB with MgActive Control1 Intervention
40 Patients - Patients will receive 30 mL of 0.25% bupivacaine with 150 mg of Mg injected below the serratus anterior muscle in the caudal direction using ultrasound guidance.
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Who is running the clinical trial?
Wayne State UniversityLead Sponsor
307 Previous Clinical Trials
108,363 Total Patients Enrolled
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