Health Condition 1: null- postoperative analgesia
Conditions
Interventions
Intervention1: group 2 Modified Pecs group: Received modified pec block, 10ml 0.5% Ropicacaine for the Pec 1 and 20 ml,0.5% Ropivacaine for Pec 2, as single dose.
Control Intervention1: group 1 - tho
Sponsors
Regional cancer centre
Eligibility
Inclusion criteria
Inclusion criteria: 1.ASA I,II, 2.BMI 18 - 35 kg/m2 3.scheduled for Modified Radical Mastectomy 4.informed written consent were included in the study.
Exclusion criteria
Exclusion criteria: pre existing local site infection,coagulopathy , morbid obesity(BMI >35),allergy to local anaesthetic,spine or chest wall deformity,pregnant women were excluded from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numerical Rating Scale, 24 hr. Morphine , Paracetamol consumption,Secondary outcome safety of blocks ,all patients were monitored for any block related complication ,pnemothorax, hypotension,local anaethetic toxicity,vascular puncture, intrathecal spread or the drug .Timepoint: Numerical Rating Scale, 24 hr. Morphine , Paracetamol consumption | — |
Secondary
| Measure | Time frame |
|---|---|
| COMPLICATIONS DUE TO THE BLOCK PROCEDURE, BLOCK FAILURE, PLEURAL PUNCTURE,VASCULAR PUNCTURE,PNEUMOTHORAX,LOCAL ANAESTHETIC TOXICITYTimepoint: immediately after block, 10 minutes,20minutes,30 minutes after the block,postoperative period ,1hour,2hours 4hours ,6hours after surgery. | — |
Countries
India
Contacts
Public ContactDr Viji SPillai
Regional Cancer Centre
Outcome results
None listed