A clinical study to compare the efficacy of two blocks in breast surgery
Phase 3
Completed
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2019/11/022118
- Lead Sponsor
- AIIMS RAIPUR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 66
Inclusion Criteria
1.American Society of Anesthesiologists Grade I and II
2.Scheduled for unilateral Modified Radical Mastectomy
Exclusion Criteria
1.Patients not willing to give consent
2.Patients with psychiatric disorder
3.Patients having pre-existing neurological disease
4.Patients having BMI > 30 Kg/m2
5.Infection at the injection site
6.Patients with coagulopathy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesia(time to first rescue analgesia after administration of block), total analgesic consumptionTimepoint: 0,1,2,4,8,12 and 24 hrs.
- Secondary Outcome Measures
Name Time Method Adverse effects 24 hrs. after surgeryTimepoint: 24 hrs.