Health Condition 1: D330- Benign neoplasm of brain, supratentorial Health Condition 2: C719- Malignant neoplasm of brain, unspecified Health Condition 3: O- Medical and Surgical Health Condition 4: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients between 18 â?? 65 years of age. 2. ASA grade I & II patients. 3. Patients posted for elective surgergy for supratentorial tumours
Exclusion criteria
Exclusion criteria: 1. Refusal of consent 2. Patients with history of smoking or chronic cough 3. Patients with history of upper respiratory tract infection (URI) in last 8 weeks 4. Patients with bleeding disorders 5. Previous laryngeal or tracheal surgery or pathology 6. Patients with history of gastric reflux 7. Patients with preoperative GCS 8. Patients with pulmonary disease, renal, cardiac or hepatic disorders, uncontrolled diabetes or blood pressure 9. Delayed extubation (more than 1 hr) 10. Patients with BMI > 35kg/mt2 11. Allergy to study drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the incidence of cough between preservative free 0.5% topical ropivacaine and placebo during extubation in patients undergoing supratentorial tumour surgeriesTimepoint: Till 5 minutes after extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To determine the effect of topical ropivacaine on heart rate and blood pressure(SBP,DBP,MAP) changes during emergence in patients undergoing supratentorial tumour surgeries. 2. To determine the effect of topical ropivacaine on the emergence time, extubation time and recovery time in these patients 3. To determine the effect of topical ropivacaine on the neurological recovery(modified Aldrete score) and sore throat in the early postoperative period in these patients Timepoint: Till one hour after extubation | — |
Countries
India
Contacts
AIIMS, New Delhi