Health Condition 1: - Health Condition 2: O- Medical and Surgical Health Condition 3: O- Medical and Surgical Health Condition 4: O- Medical and Surgical
Conditions
Interventions
Intervention1: Dexmedetomidine 0.2 mcg/kg/h: Study participants will be randomized into two groups. Intervention group receiving dexmedetomidine 0.2 mcg/kg/h infusion 15 minutes before induction of an
Sponsors
Sukanta Saha
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient of age group 18-65 yrs. 2. Patient with American society of Anesthesiologists (ASA) physical grade I or II.
Exclusion criteria
Exclusion criteria: 1. Patient who refused to give consent. 2. Local site infection. 3. History of allergy to study drugs specially amide group of drugs. 4. patient taking any analgesic and anticoagulant (bleeding tendencies). 5. uncontrolled cardiovascular, central nervous system, respiratory system comorbidities and kidney disorders. 6. Psychiatric patients. 7. Anticipated difficult intubation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Haemodynamic changes (hypertension, bradycardia) and sedation effect.Timepoint: Haemodynamic changes (hypertension, bradycardia), sedation effect and sedation score (15 min, 30 min, 45 min, 60 min, 120 min). | — |
Secondary
| Measure | Time frame |
|---|---|
| Post-operative analgesia requirements.Timepoint: We will observe total analgesic requirement on patient demand in 24 hours post-operative period. | — |
Countries
India
Contacts
Public ContactN Anita Devi
Regional Institute of Medical Sciences Imphal
Outcome results
None listed