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Compare two methods for keeping the patients pain free after operation for breast cancer.

Not Applicable
Conditions
Health Condition 1: -
Registration Number
CTRI/2018/10/015889
Lead Sponsor
Postgraduate Institute of medical education and research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA I and 2 patients undergoing mastectomy

Exclusion Criteria

BMI >35

Allergy or contraindication protocol drugs

Chronic pain treated by long term opioids

Pregnancy or breast feeding

Local infection at the block site

patient refusal or incapacity

planned sub-pectoral implant reconstruction

Uncontrolled hypertension or Ischemic heart disease

Renal dysfunction

Pre-existing neurological deficits

Psychiatric illness

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Total opioid consumption.Timepoint: 1.first 24 hours
Secondary Outcome Measures
NameTimeMethod
1.Visual Analogue Pain score in Recovery <br/ ><br>2.Visual Analogue Pain score <br/ ><br>3.Incidence of nausea and vomiting rate between the two techniques. <br/ ><br>4.Incidence of chronic post mastectomy pain at six months in both groups. <br/ ><br>Timepoint: Measured at 1, 2, 4, 6, 8, 12, and 24 hours postoperatively <br/ ><br>
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