prospective randomized study
Conditions
Interventions
Group I: (Control group): 30 patients were undergoing bilateral Erector Spinae Plane Block at T7 level with 20 ml 0.25% bupivacaine + 1ml normal saline on each side.
Group II: (Dexmedetomidine group
Sponsors
faculty of medicine - menoufia university
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Gender: male and female. Patients aged between 30 and 65 years. Scheduled to undergo laparoscopic cholecystectomy. American Society of Anesthesiology (ASA) physical status classification score of I or II.
Exclusion criteria
Exclusion criteria: History of allergy to the study drugs. Inability to communicate or any other psychological problems. Sinus bradycardia. Atrioventricular (AV) block. Any contraindications to regional block.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative analgesic duration | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pain in the first 24 h post-operative Total dose of intraoperative consumption of fentanyl Total dose of rescue analgesia in the first 24hr postoperative. sedation score at recovery patient satisfaction recovery quality | — |
Countries
Africa
Contacts
Public Contactnoha afify
faculty of medicine menoufia university department of anesthesia
Outcome results
None listed