Awake Nasotracheal Fiberoptic Intubation: A Comparison of Three Techniques of Conscious Sedation with Remifentanil ,Ketamin and Propofol Without Muscle Relaxants .
Phase 2
- Conditions
- Awake Nasotracheal Fiberoptic Intubation in Temporomandibular joint disorders.Ankylosis of joint
- Registration Number
- IRCT201208061674N4
- Lead Sponsor
- Vice-Chancellery of Research and Technology, Shiraz University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
Inclusion criteria : The patients with Physical status of I and age 15 to 60 years are enrolled; Exclusion criteria : The Patients with systemic disease and or taking any medication will excluded .
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hemodynamic stability in cardiovascular patients for safe intubation. Timepoint: During the intubation procedure. Method of measurement: Blood pressure and heart rate monitoring.;Level of sedation and the patient's tolerance to the safe intubation. Timepoint: Immediately before - during - and end of Fiberoptic procedure. Method of measurement: Ramsay Sedation score (RSS).;Speed ??in performing intubation. Timepoint: End of procedure. Method of measurement: minute.
- Secondary Outcome Measures
Name Time Method Complications during intubation. Timepoint: After the procedure and 24 hours after surgery. Method of measurement: Direct observation by the doctor and the patient report.;Satisfaction of anesthesiologist for intubation. Timepoint: End of the procedure. Method of measurement: Rating of poor (0), moderate (1), good (2), high (3).;Waste of time for procedure. Timepoint: End of the procedure. Method of measurement: minute.