CTRI/2018/02/012076
Not yet recruiting
未知
A Prospective Randomized study to compare the efficacy of Propofol-Ketamine combination with Dexmedetomidine for performing Drug Induced Sleep Endoscopy(DISE) in patients of Obstructive Sleep Apnoea.
TATA Motors Hospital0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Obstructive Sleep Apnoea
- Sponsor
- TATA Motors Hospital
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All patients who give their informed consent willingly.
- •Clinical symptoms of snoring, morning headaches,tiredness,daytime sleepiness.
- •ASA status 1\-2\.
- •Apnoea\-Hypopnea Index (AHI) score greater than 5 events per hour on Polysomnography.
- •No active focus of infection in nose and throat.
- •All patients who have previously failed to respond to conservative treatment for OSA, like changes in sleep position and sleep hygiene.
- •Patients who were either intolerant or unwillingly to use continuous positive airway pressure therapy.
- •Patients with no major systemic disease.
Exclusion Criteria
- •Age \< 18 years and \>60 years.
- •Patients with high ASA score \>3\.
- •Severe OSA (AHI \>70 events/hour).
- •Morbid Obesity BMI \>30kg/m2\.
- •Patients with 2nd\-3rd degree A\-V block.
- •Known allergies against the study drugs.
- •Gross maxillary and mandibular deformities (mainly retrognathia) on lateral cephalometry.
- •Patients with psychiatric disorders.
- •Patients who have undergone previous surgical therapies for OSA.
- •Mallampati score of 3\-4\.
Outcomes
Primary Outcomes
Not specified
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