Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients belong to ASA I or II Scheduled for elective surgeries under General Anaesthesia
Exclusion criteria
Exclusion criteria: Patients with Known Allergy or hypersensitivity to Dexmedetomidine or Propofol Patients with baseline HR less than 50bpm,Hypotension Patients with Heartblocks,arrythmia Pregnant women BMI more than 35kg per square meter
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total dose of propofol required for induction of anaesthesia in mg per kgTimepoint: Measured from start of propofol administration until loss of verbal response | — |
Secondary
| Measure | Time frame |
|---|---|
| Preoperative anxiety score assessed using Amstredam Preoperative Anxiety and Information ScaleTimepoint: Before Administration of Study Drug and after 10min of administration of Study Drug;Sedation score assessed using Ramsay Sedation ScoreTimepoint: 10min After administration of Study Drug Pre induction After induction at 1min,3min,5min,10min | — |
Countries
India
Contacts
Chettinad Hospital and Research Institute