A Study To Compare The Block Characteristics Of A Drug Named Ropivacaine 0.75% Heavy And 0.5% Bupivacaine Heavy For Spinal Anaesthesia In Infraumbillical Surgeries
Phase 4
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2023/11/059573
- Lead Sponsor
- Dr R Jagadish Raj
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
2.Patient willing to give informed consent
3.ASA grade 1 and 2
4.Patients undergoing infraumbilical surgeries under spinal anaesthesia.
Exclusion Criteria
1.Patients refusing to give informed consent
2.Patients undergoing emergency surgeries
3.Patients with history of allergy to the study drugs
4.Pregnant women
5.Patients ASA grade 3,4,5
6.Patients under 18 years and over 60 years of age.
7.Infection at the site of injection
8.Sepsis
9.Spinal deformities
10.Severe hypovolemia
11.Coagulopathies
12.Raised intracranial tension
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effects of hyperbaric ropivacaine 0.75% with hyperbaric bupivacaine 0.5% on onset, duration, time to maximum sensory and motor block.maximum level of sensory block, time to 2 segment regression of sensory blockTimepoint: baseline, every minute upto 10 minutes, every 10 minutes upto end of surgery
- Secondary Outcome Measures
Name Time Method To compare the effects of the 2 drugs on heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure, saturation of oxygen & the incidence of adverse effects if any.Timepoint: baseline, every minute upto 10 minutes, every 10 minutes upto end of surgery