A study of Ropivacaine heavy and Bupivacaine heavy in hypertensive patients undergoing surgery under spinal anaesthesia
Phase 4
- Conditions
- Health Condition 1: I131- Hypertensive heart and chronic kidney disease without heart failureHealth Condition 2: I131- Hypertensive heart and chronic kidney disease without heart failureHealth Condition 3: I119- Hypertensive heart disease withoutheart failureHealth Condition 4: I119- Hypertensive heart disease withoutheart failure
- Registration Number
- CTRI/2022/06/043360
- Lead Sponsor
- IGIMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
hypertensive patients, controlled blood pressure both male and female of age group 25- 70 years undergoing surgery under spinal anaesthesia .
Exclusion Criteria
1.Patient refusal for procedure.
2.ASA grade > III, IV
3.Emergency Surgery
4.Immunocompromised patients
5.All contraindications for Regional
anaesthesia
1. Those with bleeding disorders and local sepsis.
2. Those on anticoagulant and antiplatelet agent.
3. Those allergic to amide anaesthetics.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate, Blood pressure, mean arterial pressure recordingsTimepoint: 1min, 3min, 5min, 10min,15min,30min, 45min, 60 min intraoperative and postoperative period.
- Secondary Outcome Measures
Name Time Method modified bromage score for motor block assessment, global patient satisfaction scale, and patient comfort scoreTimepoint: in the post operative period upto 3-4 hrs