Comparison of mask and standard extubation for reduction in heart related responses.
Not Applicable
- Conditions
- Health Condition 1: null- Controlled hypertensive patients
- Registration Number
- CTRI/2015/10/006286
- Lead Sponsor
- Dr R M L Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
ASA physical status Grade II (controlled hypertensives) posted for elective surgery under general anesthesia were included
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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