Health Condition 1: J38- Diseases of vocal cords and larynx, not elsewhere classified Health Condition 2: null- Patients aged 18-65 years undergoing surgery performed on the larnyx using suspension laryngoscopy
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This study will be conducted in the Department of Anaesthesiology at All India Institute of Medical Sciences after obtaining Institutional Ethics committee approval. 60 ASA I and II patients, 18-65 years, undergoing laryngotracheal procedures requiring suspension laryngoscopy, rigid bronchoscopy will be included in this study after taking informed consent
Exclusion criteria
Exclusion criteria: 1.Patients who have neurological deficit following head injury, epilepsy etc. which can interfere with entropy monitoring. 2. Patients who are morbidly obese (BMI >35kg/m2). 3. Patients on β blockers, clonidine, verapamil.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim of the study is to evaluate the effect-site concentration (Ce) of propofol needed for laryngeal surgeries by using the entropy monitor to titrate the depth of anesthesiaTimepoint: the study involves titrating intraoperative requirement of propofol | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess- 1. if the target controlled infusion (TCI) propofol requirement during total intravenous anaesthesia(TIVA) is decreased with the concomittant use of dexamedetomidine infusion 2. whether concomittant use of dexmedetomidine with the TCI-TIVA propofol results in faster awakening of patients after laryngeal surgery 3. if the concomittant use of dexmedetomidine with the TCI-TIVA propofol results in lesser intraoperative haemodynamic variations in patients undergoing laryngeal surgery.Timepoint: Intraoperative requirement of the drugs will be titrated | — |
Countries
India
Contacts
All India Institute of Medical Sciences