Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Injection Ropivacaine: 0.5% and 0.375 % Ropivacaine is administered via usg guided infraclavicular brachial plexus block and the onset of sensory block is noted in both groups
Control
Sponsors
Dr Saurav Kalita
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients age group 18 to 65 years ,of all sexes 2, ASA grade 1 and 2 3.patient with elective orthopedic surgery for arm,elbow,forearm and hand under US guided infraclavicular approach 4.Patient who are willing to give informed and written consent for the surgery.
Exclusion criteria
Exclusion criteria: 1.Patient refusal for infraclavicular brachial plexus block 2.Patient with brachial plexus neuropathies,diabetes ,any known peripheral neuropathic disease,post CVA 3.severe brochopulmonary disease 4.coagulopathies 5. severe cardiac diseases 6.pregnancy 7.intolerance or known history of allergy to one or more medications of the study 8.Patient undergoing emergency surgeries 9 local infection at the site of the block
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the time of onset of sensory block between 0.5% and 0.375 % ropivacaine Timepoint: To compare the time of onset of sensory block between 0.5% and 0.375 % ropivacaine in orthopedic patients within 30 minutes of performing the block prior to Surgery at baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.To compare the onset time of motor block 2.Intraoperative hemodynamics , 3.The requirements of supplemental anesthesia or analgesic 4.Occurrence of any complications Timepoint: To compare the onset time of motor block,Intraoperative hemodynamics , The requirements of supplemental anesthesia or analgesic and Occurrence of any complications in orthopedic patients within 30 minutes of performing the block prior to surgery at baseline | — |
Countries
India
Contacts
Public ContactDr Priyam Saikia
Gauhati Medical College and Hospital
Outcome results
None listed