Comparison of two different concentrations of Ropivacaine local anaesthetic for postoperative pain relief in abdominal hysterectomy surgeries
Phase 3
- Conditions
- Health Condition 1: N926- Irregular menstruation, unspecified
- Registration Number
- CTRI/2024/05/067730
- Lead Sponsor
- Priyadharshini S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Elective surgeries with ASA Grading 1,2 and 3
2.Patients undergoing abdominal hysterectomy
3.Weight from 50kg to 80kg
4.Height from 145cm to 165cm
Exclusion Criteria
1.Patient refusal
2.Allergic to Ropivacaine and Fentanyl
3.Local infection at the site of epidural injection
4.Coagulopathy
5.Hypovolemia
6.Patient on anticoagulant therapy
7.Uncooperative patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the VAS score at rest, movement and while coughing between the patients getting 0.1% and 0.2% ropivacaine as epidural infusion for pain reliefTimepoint: The time duration taken by the patient to complain of pain with VAS more than 3
- Secondary Outcome Measures
Name Time Method To compare haemodynamic changesTimepoint: The time duration taken for mean arterial pressure to fall less than 60;To compare the motor blockadeTimepoint: The time duration taken by the patient to complain of lower limb numbness;To compare the need for rescue analgesiaTimepoint: The time duration taken by the patient to complain pain with VAS more than 5 even after giving rescue analgesia