Clinical Trials in Egypt / NCT07360028
Recruiting
Not applicable
Efficacy of Ultrasound Guided Erector Spinae Plane Block Versus Ultrasound Guided Serratus Anterior Plane Block for Postoperative Pain Control Following Video-assisted Thoracoscopic Surgeries (VATS): Randomized Control Trial
NCT07360028 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
Post Operative Pain Control
Investigational drug(s) / intervention(s)
Erector Spinae (ESP) Block with Bupivacaine (Marcaine®)Serratus anterior plane block (SAP)
Erector Spinae (ESP) Block with Bupivacaine (Marcaine®): Ultrasound Guided Erector Spinae Plane block using 20 mL of 0.25% bupivacaine.
Serratus anterior plane block (SAP): Ultrasound Guided Serratus Anterior Plane Block using 20 mL of 0.25% bupivacaine.
Study summary
The aim of the study is to compare the analgesic efficacy of Erector spinae plane block versus Serratus anterior plane block in patients undergoing video-assisted thoracoscopic surgeries.
Eligibility
Inclusion Criteria:
* Patients with American Society of Anesthesiology physical status ASA I, II and III.
* Patients aged between 25 and 70 years.
* patients undergoing video-assisted thoracoscopic surgeries (VATS), including pleurectomy, bullectomy, sympathectomy, esophagectomy, decortication, lobectomy, and pneumonectomy.
Exclusion Criteria:
* Patients below age of 25 or above age of 70.
* Patient refusal.
* Allergy to local anesthetic drugs.
* Bleeding or coagulation disorder.
* Psychiatric disorders.
* Infection at the needle entry site.
* Renal impairment (creatinine \>1.5 ).
* Hepatic impairment (Child B or C).
* Patients with known Cortisol related diseases such as Cushing's Syndrome or Addison's Disease.
Primary outcome measure(s)
- Visual analogue scale for Assessing postoperative pain control — after ICU admission at 2, 4, 8, 16, 24 hours post operative.
Assessing The difference in postoperative pain control between both groups as determined by assessing the visual analogue scale
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Ain-Shams University Hospitals | Cairo | Abbassia-Egypt | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07360028 on ClinicalTrials.gov ↗ ← All trials in Egypt