Comparative study between local anesthetic and local anesthetic with an adjuvant for regional block using ultrasound for post operative pain relief in elective Hysterectomy cases
Not Applicable
- Conditions
- Health Condition 1: N948- Other specified conditions associated with female genital organs and menstrual cycle
- Registration Number
- CTRI/2021/10/037175
- Lead Sponsor
- Vijayanagar Institute Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. All patients coming for elective Total Abdominal Hysterectomy under spinal anaesthesia
2. ASA physical status I and II
Exclusion Criteria
1. Refusal by patients for the procedure
2. Allergy to study drugs
3. History of significant systemic disorders(cardiovascular, respiratory, central nervous system or renal system)
4. Emergency surgeries
5. Spinal deformities
6. Patients with bleeding diathesis
7. Local skin site infection
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine duration of post operative analgesiaTimepoint: Within 24 hrs of giving block
- Secondary Outcome Measures
Name Time Method 1.Quality of analgesia assessed by NRS pain score at rest,movement,cough <br/ ><br>2. 24 houranalgesic consumption(tramadol IV) <br/ ><br>3. Hemodynamic parameters(BP and pulse) <br/ ><br>4. Oxygen saturation <br/ ><br>5. Sedation(Modified Ramsay sedation score) <br/ ><br>6. Post operative nausea and vomiting and any other complication.Timepoint: In 24 hrs