Health Condition 1: null- CARCINOMA BREAST
Conditions
Interventions
Intervention1: Group S: Modified radical mastectomy under general anaestheisa along with SAP block
using 0.4ml/kg of 0.375% Ropivacaine(with a maximum volume of 30ml)
Control Intervention1: NIL: N
Sponsors
AIIMS
Eligibility
Inclusion criteria
Inclusion criteria: American society of anesthesiologistâ??s (ASA) physical status (PS) I and II undergoing modified radical mastectomy will be recruited in this study.
Exclusion criteria
Exclusion criteria: 1. Unwilling patients 2. Patients with infection at the site of SAPblock. 3. Patient withsevere chest wall deformity. 4. Patient with BMI >=30kg/m2. 5. Patients with history suggestive of coagulopathy or receiving any anticoagulants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to first rescue analgesic in the post-operative period in women undergoing modified radical mastectomy under general anaesthesia with and without SAP block.Timepoint: Pain assessment will be done in the immediate postoperative period after shifting the patient to PACU(time zero) and thereafter at 1, 2, 6, 12 and 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| â?¢ Total intraoperative fentanyl consumption among the two groups. â?¢ Total doses of diclofenac consumed in the post operative period in 24 hours. â?¢ Total tramadol consumption in mg in the post operative period in 24 hours. â?¢ Postoperative nausea and vomiting Timepoint: Nausea and vomiting will be measured at 0, 1, 2, 6, 12 and 24 hours and whenever the patient complains of nausea/vomiting | — |
Countries
India
Contacts
Public ContactDr Swati Bhan
DrBRAIRCH, AIIMS
Outcome results
None listed