To study the potency of pain relief provided by the nerve block given with two drugs under ultrasound guidance in patients who have thigh bone fracture before positioning them for spinal anaesthesia.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/01/039069
- Lead Sponsor
- Dr Sahana S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients posted for surgeries for femur fracture. American Society of Anaesthesiologists (ASA) class 1 and 2 patients.
Exclusion Criteria
Patients with history of kown allergy to bupivacaine or dexmedetomidine, pregnancy and lactation, pre-existing neurological conditions, alcoholism, drug abuse, psychological or other emotional problems that are likely to invalidate the informed consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain score in terms of visual analogue scale and numerical rating scale of lesser than or equal to 3Timepoint: 20 minutes after fascia iliaca compartment block, during positioning for spinal anaesthesia
- Secondary Outcome Measures
Name Time Method to assess the sedation in terms of Ramsay Sedation ScoreTimepoint: perioperative period