Scalp Block Versus Scalp Infiltration With Dexmedetomidine and Local Anesthetic for Post Craniotomy Pain
Headache
About this trial
This is an interventional prevention trial for Headache focused on measuring dexmedetomidine, nerve block, anesthesia infiltration
Eligibility Criteria
Inclusion Criteria:
- Neurosurgical patients
- 18-70 years of age
- ASA class I and II
- Patients undergoing elective craniotomy, who were conscious and oriented to time, person and place and able to understand and use Numerical Rating Scale (NRS)
Exclusion Criteria:
- Patient dull and irritable
- GCS <15
- Craniotomy incision extending beyond scalp (the field of the block) e.g. craniofacial surgery
- Patients treated chronically with analgesics or narcotic medications
- Allergy to local anaesthetics or dexmedetomedine
- Patients planned for post-operative mechanical ventilation
Following patients were excluded from the study during collection of data in the postoperative period:-
- Patients developing fever (≥39°C) in the postoperative period
- Requiring postoperative ventilation (unplanned)
- Having poor cognitive function at 1 hour postoperative period
- GCS <15 in post-operative period.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Active Comparator
Bupivacaine,dexmedetomidine scalp block
bupivacaine dexmedetomidine infiltration
bupivacaine infiltration
Bupivacaine (0.25%) and Dexmedetomedine (1 µg/kg). Maximum dose of bupivacaine kept < 2 mg /kg for scalp block
The incision site was infiltrated with 15-20 ml bupivacaine (0.25%) and dexmedetomedine (1 µg/kg). {1/3rd in the muscle and 2/3rd in the subcutaneous tissue}. Maximum dose of bupivacaine kept less than 2 mg /kg.
The incision site was infiltrated with 15-20 ml of bupivacaine (0.25%). {1/3rd in the muscle and 2/3rd in the subcutaneous tissue}. Maximum dose of bupivacaine kept less than 2 mg /kg.