Health Condition 1: null- Controlled hypertensive patients
Conditions
Interventions
Intervention1: pro seal laryngeal mask airway extubation: extubation performed over pro seal laryngeal mask airway device. The study shall be carried for a duration of 3 months
Control Intervention1:
Sponsors
Dr R M L Hospital
Eligibility
Inclusion criteria
Inclusion criteria: ASA physical status Grade II (controlled hypertensives) posted for elective surgery under general anesthesia were included
Exclusion criteria
Exclusion criteria: Patients with a history of pulmonary disease like COPD, asthma, pregnancy, morbid obesity, diabetes mellitus (HbA1c >6.5%), long duration surgeries ( >4 hours with major fluid shifts), impaired kidney or liver function, anticipated difficult airway, progressive neurological disease and bleeding diathesis were excluded from this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The parameters monitored as primary outcome during the study were heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP) and mean blood pressure (MBP).Timepoint: The parameters monitored as primary outcome during the study were heart rate (HR), systolic blood pressure (SBP), diastolic blood pressure (DBP) and mean blood pressure (MBP). Measured on arrival in OT, before extubation and at 1, 3, 6, 8,10 minutes after extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes were 5 lead electrocardiogram (ECG), oxygen saturation by pulse oxymetry and end tidal carbon dioxide (ETCo2) by capnography.Timepoint: 1, 3, 6, 8 and 10 minutes | — |
Countries
India
Contacts
Public ContactDr Michell Gulabani
Dr R P Singh
Outcome results
None listed