Health Condition 1: C50- Malignant neoplasm of breast
Conditions
Interventions
Intervention1: Complete Antethoracic Block: Patients will receive Complete
Antethoracic block with 60ml
0.2% ropivacaine along with
general anaesthesia.
Control Intervention1: Thoracic Paravertebral b
Sponsors
AIIMS
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. BMI > 35kg/m2 2. Patient with infection at the site of injection 3. Coagulopathy 4. Spine deformity 5. Drug addicts or history of opioid dependence 6. 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 rescue analgesia after administration of block ). Timepoint: Post-operative (0 min) ,30 min ,1, 2 , 6 ,12 and 24 hours or as per patients request within 24hours in postoperative period | — |
Secondary
| Measure | Time frame |
|---|---|
| Total rescue analgesic requirement in Post-operative period. Timepoint: Post-operative (0 min) ,30 min ,1, 2 , 6 ,12 and 24 hours or as per patients request within 24hours of surgery;Comparison of Post-operative pain ( using numeric rating scale) and adverse effectsTimepoint: Post-operative (0 min) ,30 min ,1, 2 , 6 ,12 and 24 hours;To evaluate and compare patient satisfaction with the block procedure and at the end of 24hours in postoperative period.Timepoint: Immediately after the block and at the end of 24hours in postoperative period. | — |
Countries
India
Contacts
Public ContactDr Sachidanand Jee Bharti
Dr B.R.A.I.R.C.H.,All India Institute of Medical Sciences,New Delhi
Outcome results
None listed