Health Condition 1: D249- Benign neoplasm of unspecified breast Health Condition 2: C509- Malignant neoplasm of breast of unspecified site Health Condition 3: C269- Malignant neoplasm of ill-definedsites within the digestive system Health Condition 4: C55- Malignant neoplasm of uterus, partunspecified
Conditions
Interventions
Intervention1: INJ Sugammadex: a single
intravenous (IV) dose of INJ Sugammadex (2.0 mg/kg)
Control Intervention1: INJ Neostigmine plus INJ Glycopyrrolate: a single IV
dose of INJ Neostigmine 0.05mg
Sponsors
Dr Eashwar S M
Eligibility
Inclusion criteria
Inclusion criteria: Patients consenting to participate in the study. ASA Grade I & II patients. BMI less than 30kg/m2
Exclusion criteria
Exclusion criteria: Patient not consenting to the study. ASA III & IV Patients with neuromuscular disorders. Hypersensitivity/ allergic history to drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of Sugammadex versus Neostigmine for reversal of NMB induced by Rocuronium.Timepoint: 5hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the adverse effects of Sugammadex versus Neostigmine.Timepoint: 5 hours | — |
Countries
India
Contacts
Public ContactDr Punita priya S
kidwai memorial institute of oncology
Outcome results
None listed