Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Control Intervention1: Patients receiving Isobaric Inj.Ropivacaine 0.75% 3.5 ml with 1mg Inj.Nalbuphine(0.1ml) diluted till 0.5 ml with sterile NS.: level of sensory block will be assessed at 2 and 5
Sponsors
Smt Bhikiben Kanjibhai Shah Medical Institute and Research Center
Eligibility
Inclusion criteria
Inclusion criteria: Patient willing to sign informed consent. ASA I & ASA Ill patients undergoing infraumbilical surgeries. Patients in the age between 18- 65 years. No known history of allergy, sensitivity or other form of reaction to local anesthetics of the ester and amide type and to opioids
Exclusion criteria
Exclusion criteria: Patient refusal. Allergy to any drugs. History of seizure disorder. Known allergy to trial drug. Patients with neurological disorders and neuropathies or receiving medications known to influence neuromuscular junction. ASA III, IV, Patients. Any contraindication to Spinal Anaesthesia (local site infection, spine deformity, clotting abnormalities)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This observational study will help us to evaluate whether Ropivacaine with Tramadol or Ropivacaine with Nalbuphine intrathecally is better for infra-umbilical surgeriesTimepoint: level of sensory block assessed at 2 and 5 min post injection and at 5 min interval till 15 minutes. onset of sensory block and duration of sensory block. assessment of motor blockae using bromage scale,time of onset(time from from intrathecal injection to chieve grae 1 motor block)and Duration of sensory block(time from intrathecal injection to reurn of sensation at L1) assessment of motor blockade using time of onset and duration of motor block | — |
Countries
India
Contacts
Public ContactDr Dinesh Chauhan
Smt. Bhikiben Kanjibhai Shah Medical Institute and Research Centre
Outcome results
None listed