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comparison of two blocks for pain relief in modified radical mastectomy

Phase 2
Conditions
Health Condition 1: C508- Malignant neoplasm of overlappingsites of breast
Registration Number
CTRI/2019/09/021030
Lead Sponsor
PGIMER Dr RML Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All female patients in the age group of 18-80 years scheduled to undergo modified radical mastectomy under general anesthesia

Exclusion Criteria

Local infection at the block site, coagulopathy, allergic to local anesthetic, bleading disorders, pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time of first rescue analgesic requirementTimepoint: time of administration of block and the time patient complaints of pain
Secondary Outcome Measures
NameTimeMethod
Average Visual Analog Score in 12hrs, total rescue analgesic requirement in 12hrs, intraoperative and postoperative hemodynamic changes, complicationsTimepoint: 30 minutes, 2nd hour, 4th hour, 8th hour and 12th hour
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