se of local anaesthetic for Quadratus Lumborum muscle Block in patients undergoing surgical removal of uterus and its effect on requirement of post operative pain relief medications
Phase 4
Completed
- Conditions
- Health Condition 1: null- patients undergoing Total Abdominal HysterectomyHealth Condition 2: N949- Unspecified condition associated with female genital organs and menstrual cycle
- Registration Number
- CTRI/2017/02/007905
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
1. Females suffering from pathology requiring total abdominal hysterectomy
2. American Society of Anesthesiologists physical status I-II
Exclusion Criteria
1. History of relevant drug allergy
2. History of psychiatric illness, substance abuse
3. Severe cardiovascular, respiratory, liver diseases metabolic or neurological disease
4. Chronic treatment with analgesics
5.Coagulopathy
6.Infection at planned injection site
7.Psychological inability of the patient to understand visual analogue scale
8.History of intake of drugs such as imipramine, theophylline, fluvoxamine and antiarrhythmic agents
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To analyze the intensity of post-operative pain relief in both groups by visual analogue scaleTimepoint: 30mins, 1hr, 4hrs, 8hrs, 12hrs, 24hrs, 36hrs and 48 hrs.
- Secondary Outcome Measures
Name Time Method To analyze total cumulative morphine consumption in both the groups over 48 hoursTimepoint: 30mins, 1hr, 4hrs, 8hrs, 12hrs, 24hrs, 36hrs and 48 hrs.