To study about the post operative analgesia in participants receiving Intrathecal 0.75% hyperbaric ropivacaine with demeditomidine vs clonidine for lower limb surgeries among 27 participants in each group.A randomized control study
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065890
- Lead Sponsor
- JSS Academy of Higher Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age 18-60 years
Either sex
ASA status I & II
Patients undergoing Lower Limb surgeries
Exclusion Criteria
1)Patient refusal for procedure
2)Spinal anomalies
3)Any contraindications to spinal anaesthesia such as local infection at site of injection,allergy to drug,raised intracranial pressure,deranged coagulation profile.
4)ASA status III and above
5)Pregnant patients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To Compare the effectiveness of duration of analgesia, Onset of sensory block till T-10,Intraoperative Hemodynamic changes, Onset of motor blockade, Time to first rescue analgesia, Incidence of adverse events such as nausea & vomiting in postoperative period.Timepoint: From time of spinal anaesthesia and noted at 0 minutes 5 minutes till 210 minutes.Tilt patient feel pain at incision site.
- Secondary Outcome Measures
Name Time Method Onset of sensory block till T-10,Intraoperative Hemodynamic changes, Onset of motor blockade, Time to first rescue analgesia, Incidence of adverse events such as nausea & vomiting in postoperative period.Timepoint: From time of spinal anaesthesia & noted at 0 minutes 5 minutes till 210 minutes.Tilt patient feel pain at incision site.