Breast Cancer Clinical Trial
Official title:
Addition of Dexmedetomidine to Ropivacaine for Ultrasound Guided Erector Spinae Block: Evaluation of Effect on Postoperative Pain After Breast Surgery: A Double-Blinded, Prospective, Randomized Clinical Trial
Patients undergoing Partial or total mastectomy with axillary LN dissection will receive prior to induction of general anaesthesia ESP block at T4 level at the same side of the surgery. one group will receive ropivacaine 0.375% and the other will get ropivacaine 0.375% with dexmedetomidine 0.5mcg/kg as an adjuvant. time to first narcotic requirement will be documented and therefore an assessment of the duration of action of the block will be made
Status | Recruiting |
Enrollment | 44 |
Est. completion date | January 17, 2022 |
Est. primary completion date | July 17, 2021 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. ASA class I, II and III patients 2. Age range: 18-80 years old 3. Elective partial or unilateral radical mastectomy with sentinel lymph node dissection Exclusion Criteria: 1. Pregnant woman 2. Bilateral mastectomy. 3. Skin infection at the site of needle puncture 4. Coagulopathy problems 5. Allergy or contraindication to any of the study drugs 6. Recent use of opioid drugs |
Country | Name | City | State |
---|---|---|---|
Lebanon | Lebanese American University Medical Center-Rizk Hospital | Beirut |
Lead Sponsor | Collaborator |
---|---|
Lebanese American University |
Lebanon,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain assessment in the first 24 hours post operatively: VAS score | Pain will be assessed using the VAS score ranging from 0, indicating no pain at all, to 10, indicating the worst pain the patient has ever felt | 24 hours |
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