Sub costal Transverus Abdominal Plane Block.
Conditions
Interventions
Intervention 1: Intervention group:This randomized study will be enrolled patients with American Society of Anesthesiologists (ASA) physical status I–II aged 18–65 years, undergoing laparoscopic chole
Sponsors
Zanjan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients within 20-60 years undregoing laparoscopic Cholecystectomy Body Mass Index below 30
Exclusion criteria
Exclusion criteria: pregnancy Allergy to local anesthetics sepsis Addiction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain rating in Visual Analogue Scale. Timepoint: During recovery,At 4h,8h,12h,24h after surgery. Method of measurement: Visual Analogue Scale questionnaire.;Post operative need to opioid analgesic. Timepoint: During recovery,At 4h,8h,12h,24h after surgery. Method of measurement: Opioid amounts(mg).;Post operative Nausea and vomiting. Timepoint: During recovery,At 4h,8h,12h,24h after surgery. Method of measurement: Categorical Scoring System for nausea. | — |
Secondary
| Measure | Time frame |
|---|---|
| Need to postop analgesic. Timepoint: During recovery,At 4h,8h,12h,24h after surgery. Method of measurement: Analgesic amounts(mg). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSaeed Jalili
Zanjan University of Medical Sciences
Outcome results
None listed