Health Condition 1: - Health Condition 2: C509- Malignant neoplasm of breast of unspecified site Health Condition 3: O- Medical and Surgical
Conditions
Interventions
Intervention1: 0.25% Bupivacaine and 1% Lignocaine: USG guided PEC 1 and PEC 2 Block using solution of 20ml of 0.25% Bupivacaine and 20ml 1% Lignocaine with Adrenaline
Control Intervention1: IV F
Sponsors
Goa medical college and hospital
Eligibility
Inclusion criteria
Inclusion criteria: BMI: 18-25 ASA Status: I, II Surgery: Surgery for Cancer of Breast Informed Consent
Exclusion criteria
Exclusion criteria: Pregnant& lactating women History of allergy to Dexmedetomidine, Lignocaine,Bupivacaine Patient on treatment with Beta blockers, HR Epilepsy/ seizures Obstructive sleep apnea
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of Opioid Anaesthesia (OA) and Opioid free Anaesthesia (OFA) in reducing pain scores, postoperatively, in breast cancer surgery. Pain will be assessed by visual analogue scale (VAS) score.Timepoint: VAS will be assessed at 0, 2, 4, 6, 12, 24 hours postoperatively | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare 1. Intraoperative hemodynamic parameters 2. Discharge time from Recovery Room 3. Duration of postoperative analgesia 4. Analgesia requirement in the postoperative periodTimepoint: Intraoperative parameters Stay in recovery room Analgesia used post operative upto 24hours | — |
Countries
India
Contacts
Public ContactDr Shirley Ann DSouza
Goa medical college and hospital
Outcome results
None listed