pain relief after breast cancer surgery with blocks
- Conditions
- Health Condition 1: null- Breast Cancer undergoing modified radical mastectomyHealth Condition 2: C50-C50- Malignant neoplasms of breast
- Registration Number
- CTRI/2018/05/013961
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 66
Patients belonging to American Society of Anesthesiologists (ASA) physical status grade I and II, aged between 25 to 85 years, scheduled to undergo MRM
1.Patient refusal
2.Preexisting infection at block site
3.Coagulation Disorder
4.Preoperative hypotension (Mean arterial blood pressure < 50 mmHg), preoperative bradycardia (Heart rate < 45 beats/min) and preoperative dysrhythmia.
5.History of psychiatric illness and preexisting neurological deficits
6.Patient with morbid obesity BMI >40 kg/ m2
7.Pregnant patients
8.Decreased pulmonary reserve, cardiac disorders and renal dysfunctions
9.Known allergy to study drugs
10.Patient with fungating growth or growth with infection at site of block
11.Patient posted for repeat surgery.
12.Presence of any preoperative pain or history of chronic pain
13.History of regular analgesic use
14.History of pre operative radiotherapy and chemotherapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of our study will be to assess pain, using visual analogue scale in post operative period for 24 hoursTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method The secondary outcome will be to assess and compare duration of analgesia (time to use first rescue analgesic), total amount of rescue analgesic used during 24 hours, duration to perform block, incidence of procedure related complications and postoperative complications, failure rate and patient satisfaction.Timepoint: 24 hours