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Evaluation of effectiveness of blocking nerve supply to breast and axilla intraoperatively for post operative pain relief after breast surgery

Phase 4
Completed
Conditions
Health Condition 1: null- Breast cancer patients
Registration Number
CTRI/2017/03/008209
Lead Sponsor
Dr Mary Thomas
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

1. All ASA PS 1& 2 patients posted for modified radical mastectomy and breast conservative surgery

2. Patients with stage I, II, III disease

3. No residual Disease at end of surgical resection

Exclusion Criteria

•Local anaesthetic allergy

•BMI >40 Kg/ m2 and < 15 kg/m2

•Fungating breast

•Bleeding dyscrasias and patients on anticoagulants

•Tumor infiltrating chest wall

•Diabetic neuropathy

•Patients on anticonvulsants

•Chemotherapy induced peripheral neuropathy

•Neurologic deficits

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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