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A study to assess the usefulness of a block technique in breast surgeries in terms of pain and related hormonal changes in blood.

Not Applicable
Conditions
Health Condition 1: C50- Malignant neoplasm of breast
Registration Number
CTRI/2018/10/015897
Lead Sponsor
AIIMSPatna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

ASA I/II patients undergoing unilateral MRM

Exclusion Criteria

a) Refusal to give consent

b) ASA III or more

c) Patients with sepsis.

d) Coagulopathy disorder.

e) Allergic to drug.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the effect of ultrasound guided ES block on the modification of the surgical neuroendocrine stress responseTimepoint: 0 minutes, 15 minutes, 30 minutes (after surgery), 24 hours (after surgery)
Secondary Outcome Measures
NameTimeMethod
total amount of opioid consumptionTimepoint: 24 hours after surgery
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