Comparison of two drugs for intubating during awake fiberoptic broncoscopy in oral carcinoma surgeries
Phase 1
- Conditions
- Health Condition 1: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx
- Registration Number
- CTRI/2024/04/065255
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients included in the study should meet the following inclusion criteria-
Age- 18-70 years of either gender
ASA physical status -I or II
Type of surgery- Oral carcinoma surgery
Nature of surgery-Elective
MP grade III &IV
Type of anaesthesia- General Anaesthesia
Patients giving written informed consent
Exclusion Criteria
Patient Refusal
MP grade I &II
ASA III &IV
Allergy to drug
Major cardiorespiratory disease
Emergency surgeries
Difficult mask ventilation
Nasal mass
Coagulation disorder
Hepatic or renal disease
Pregnant patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare intubating conditions among two groups with intubation score Coughing and post intubation scoreTimepoint: 4 hrs
- Secondary Outcome Measures
Name Time Method To compare haemodynamic parameters among two groups. <br/ ><br>To compare sedation (Ramsay sedation score) among two groups. <br/ ><br>Timepoint: 0 min to 2hrs