A clinical study to compare the efficacy of three different blocks for pain relief in breast surgeries
Not Applicable
- Conditions
- Health Condition 1: C50- Malignant neoplasm of breast
- Registration Number
- CTRI/2023/02/049932
- Lead Sponsor
- SRM Medical College Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Patients undergoing unilateral modified radical mastectomy
2)ASA I & II
Exclusion Criteria
1)Patients undergoing repeated breast surgeries
2)Patients with cardiac diseases, chronic kidney diseases, chronic liver diseases, respiratory diseases and neurological diseases
3)Patients with deranged coagulation profile
4)Patients with allergy to local anesthetics
5)Patients with substance or alcohol abuse
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare morphine consumption in 24 hours postoperatively <br/ ><br>Timepoint: To compare morphine consumption in 24 hours postoperatively <br/ ><br>
- Secondary Outcome Measures
Name Time Method Comparison of VAS scores in the 24 hour postoperative period. <br/ ><br>Timepoint: The hourly VAS scores of the patient in the 24 hour postoperative period will be noted;Intraoperative fentanyl requirement <br/ ><br>Timepoint: The total amount of Fentanyl given to the patient in the intraoperative period will be noted;Time to the first rescue analgesia <br/ ><br>Timepoint: The time taken for the patient needing first analgesic reqirement will be noted