Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA physical status I and II Duration of surgery is less than 2 hours
Exclusion criteria
Exclusion criteria: Patients refusing to participate in the study Patients with known neuromuscular disorders Patients undergoing organ transplant surgery emergency procedures and patients needing intensive care admission in the postoperative period Obese patients with a body mass index BMI greater than 30kg/m2 Renal or hepatic dysfunction Women taking oral contraceptives Pregnant patients Allergy to drugs under study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time required to achieve the quantitative neuromuscular monitoring endpoint (TOFR 0.9) following the administration of the reversal agents under investigationTimepoint: At time of giving reversal agent When TOFR reached 0.9 | — |
Secondary
| Measure | Time frame |
|---|---|
| patients having bronchospasm, tachypnea with respiratory rate greater than 24 per min, SpO2 less than 92 % at room air during the first 60 min after extubation, in the PACU. patients requiring airway support (viz. airway opening manoeuvres, oral or nasal airway insertion, CPAP / BiPAP, endotracheal intubation) during the first 60 min after extubation, in the PACU. patients having heart rate greater than 100/min or less than 60/min, systolic blood pressure plus minus 20% of baseline, diastolic blood pressure plus minus 20% of baseline, and mean blood pressure plus minus 20% of baseline, after administration of reversal agent, continuing to PACU for the first 60 min post-extubation. Timepoint: till 60 mins after extubation | — |
Countries
India
Contacts
Institute of Anaesthesiology, Pain and Perioperative Medicin