Health Condition 1: null- Patients with breast cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. ASA I and II 2. Patients posted for MRM 3. Patients giving written informed consent to participate in the study
Exclusion criteria
Exclusion criteria: 1. Patient refusal 2. Age 70 years 3. Patients with BMI > 35kg/m2 4. Patient with infection at the site of injection 5. Coagulopathy 6. Spine deformity 7. Drug addicts or history of opioid dependence 8. Patients with history of allergy to opioids or local anaesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To measure the duration of post-operative analgesia (that is, time to first analgesic request from the time of giving block ). Timepoint: Pain assessment would be done in immediate post (0 min), 30 min, 1 hr , 2hr , 6hr, 12 and 24 hr. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Total rescue analgesic requirement in postoperative period. 2) To evaluate patient satisfaction in postoperative period. Timepoint: Patient satisfaction would be evaluated at 24 hrs after surgery | — |
Countries
India
Contacts
AIIMS , NEW DELHI