Health Condition 1: X58- Exposure to other specified factors
Conditions
Interventions
Intervention1: Subarachnoid Block Using Spinal Needle: For Group A: Hyperbaric Levobupivacaine (3ml) and for Group B: Hyperbaric Ropivacaine (3ml) will be given under Aseptic conditions using Spinal N
Sponsors
LLRM Medical College
Eligibility
Inclusion criteria
Inclusion criteria: ASA GRADE I and II Age between 18 to 65 years Patients undergoing lower limb Surgeries
Exclusion criteria
Exclusion criteria: Patient Refusal Infection at the Injection Site Coagulopathy Increased Intracranial Pressure Known Allergy or Hypersensitivity to Local Anaesthetic Agents
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is to study the efficacy of the drug based on Duration of motor blockade , assessed by Modified Bromage scale.Timepoint: Baseline vitals will be noted. After Spinal anesthesia, Haemodynamic parameters ( SBP,DBP,MAP,HR), Loss of sensory and motor function will be noted every 1 minute for first 5 minutes, every 2 minutes for next 10 minutes, every 5 minutes for next 25 minutes and then every 30 minutes till regression of block. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To compare and Evaluate Onset of sensory block in both the groups 2.To compare and Evaluate Onset of motor block in both the groups 3.To compare and Evaluate Duration of Motor block in both the groups 4.To compare and Evaluate time of first rescue Analgesia in both the groups 5.To compare hemodynamic changes if any 6.Complications if any in both the groupsTimepoint: Baseline vitals will be noted. After Spinal anesthesia, Haemodynamic parameters ( SBP,DBP,MAP,HR), Loss of sensory and motor function will be noted every 1 minute for first 5 minutes, every 2 minutes for next 10 minutes, every 5 minutes for next 25 minutes and then every 30 minutes till regression of block. | — |
Countries
India
Contacts
Public ContactDr Neelam Singh
Llrm medical college
Outcome results
None listed