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NCT05429489 Clinical Trial

Erector Spinae Plane Block Versus General Anesthesia in Breast Cancer Surgeries

Analgesia Clinical Trial

Official title:
Comparison of the Efficacy of Bilevel Erector Spinae Plane Block and Single Level Erector Spinae Plane Block Versus General Anesthesia in Breast Cancer Surgeries

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05429489
Other study ID # AP2205-5015
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 27, 2022
Est. completion date January 10, 2024

Study information
Verified date January 2024
Source National Cancer Institute, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims at comparing the analgesic efficacy and safety of bilevel erector spinae versus single level versus general anesthesia for breast cancer surgeries

Recruitment information / eligibility
Status Completed
Enrollment 126
Est. completion date January 10, 2024
Est. primary completion date December 27, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Female - Diagnosed with breast cancer Exclusion Criteria: - Patient refusal - coagulation defects - bone metastases - abnormal kidney and/or liver function tests

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Bilevel erector spinae plane block
Bilevel erector spinae plane block at 3rd and 5th thoracic vertebral levels
• Single level erector spinae plane block
Single level erector spinae plane block at 5th thoracic vertebrae
Drug:
• Intravenous morphine
Intravenous morphine 0.1 mg/kg

Locations
Country Name City State
Egypt Walaa Y Elsabeeny Cairo

Sponsors (1)
Lead Sponsor Collaborator
National Cancer Institute, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Total analgesic requisite total postoperative morphine consumption First 24 hours postoperatively
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