Health Condition 1: null- asa 1 and 2 patients scheduled for elective modified radical mastectomy Health Condition 2: C50- Malignant neoplasm of breast
Conditions
Interventions
Intervention1: 1. paravertebral block
2. Pectoralis 2 block
3 serratus anterior plane block: 1. 20 ml 0.375% ropivacaine
2. 30 ml 0.375% ropivacaine
3. 30 ml 0.375% ropivacaine
Intervention2: PECS II
Sponsors
All India Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: ASA 1 and 2 undergoing elective mastectomy surgeries
Exclusion criteria
Exclusion criteria: coagulopathy BMI >35kg/m2 pregnancy mental retardation chest wall deformity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Find out the spread of local anesthetic radiographically and co-relate it with the sensory blockade produced. 2.To compare the post operative 24 hour fentanyl consumption. Timepoint: 1.radiographic spread seen immediately after injecting the drug. sensory block seen 15-30 minutes after injecting the drug 2.total fentalyl consumption seen at 24 hours after the surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| â?¢Onset of sensory blockade â?¢Intra-operative opioid requirement â?¢Visual Analog Scale (VAS) scores for pain for 24 hours post operative period â?¢Time for first post operative analgesia requirement â?¢Incidence of post operative nausea and vomiting (PONV) Timepoint: specified in the outcomes Post operative nausea vomiting for 24 hours post op | — |
Countries
India
Contacts
Public ContactDhruv jain
All india institute of medical sciences, New Delhi
Outcome results
None listed