study of hyperbaric Ropivacaine and hyperbaric levo Bupivacaine for subarachnoid block in lower limb orthopaedic surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061853
- Lead Sponsor
- RIMS, RANCHI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) 18 to 65 years of either sex
2) Weight of 45 to 75 kgs
3)Height of 150 to 180cms
4) Patients undergoing lower limb orthopaedic surgery
5) ASA grade I & II
Exclusion Criteria
1)Patient unwilling
2)Any bleeding disorder and patient on anticoagulants.
3) Neurological and musculoskeletal disease.
4) History of any allergy to local anaesthetic agents and signs of allergy to lidocaine test dose.
5)Significant history of drug/alcohol abuse
6) Patients with contradindication for regional anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to determine the time of onset, time to attainment of maximum level, maximum level attained & duration of sensory blockade. <br/ ><br>Timepoint: From the time of giving subarachnoid block till the end of surgery and postoperative period (6hrs) <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1)To determine the time of onset, time to attainment of maximum bromage score, maximum bromage score reached and duration of motor blockade. <br/ ><br>2)To assess the hemodynamic changes like- blood pressure, heart rate, urine output during the period of spinal anesthesia. <br/ ><br>3)To enhance patients safety and faster recoveryTimepoint: From the time of giving subarachnoid block till the end of surgery and postoperative period (12hrs) <br/ ><br>