None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult patients aged 18 65 years. ASA physical status I,II & III. Patients scheduled for Elective Laparoscopic Colorectal and Robot assisted Laparoscopic Abdominal surgeries
Exclusion criteria
Exclusion criteria: Known neuromuscular disorders Severe hepatic or renal impairment Pregnancy or lactation. Known hypersensitivity to neuromuscular blocking agents. Patients on medications affecting neuromuscular transmission Body Mass Index greater than 35
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the mean time required to attain TOF ratio greater than or equal to 0.9 after stopping Cisatracurium infusionTimepoint: TOF will be assessed every 10 minutes after stopping Cisatracurium Infusion | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the time required to attain a TOF ratio 0.9 after administration of reversal agentsTimepoint: Reversal agents will be administered after TOF attains 0.7. After that every 10 minutes we assess TOF till it reaches 0.9; To quantify intraoperative opioid requirements & analyze their association with depth of neuromuscular blockade & recovery profile.Timepoint: Opioids will be administered intraoperatively based on Hemodynamic changes due to painful stimulus; To measure the minimum alveolar concentration (MAC) during maintenance anesthesia & study its relationship with neuromuscular blockade depthTimepoint: Intraoperative Mean Alveolar Concentration of Inhalational Agents will be measures every 30 minutes after starting Cisatracurium infusion till the infusion will be discontinued; To quantify intraoperative Neuromuscular Bolus requirementsTimepoint: Neuromuscular Bolus will be administered of the usual infusion dosage is not enough for maintaining T1 value equals to 10 percentage | — |
Countries
India
Contacts
Senior Professor