Comparison of two ultrasound guided blocks in relieving post operative pain after hip fracture surgeries
- Conditions
- Fracture of head and neck of femur, (2) ICD-10 Condition: S721||Pertrochanteric fracture, (3) ICD-10 Condition: S722||Subtrochanteric fracture of femur,
- Registration Number
- CTRI/2019/03/017975
- Lead Sponsor
- VMMC and Safdarjung Hospital
- Brief Summary
The proposed study will be conducted in the Department of Anaesthesia and Intensive Care, Vardhman Mahavir Medical College, New Delhi, after obtaining written informed consent from all the patients.
All patients will undergo a pre-anaesthetic check up with all the relevant investigations.
Following the application of the blocks, the patients will be taken up for surgery after giving a subarachnoid block using hyperbaric 0.5% bupivacaine (2.5 ml) + fentanyl (15 microgram).
Monitoring of the level of block will be done during surgery and when the level of sensory block recedes to T10, 25ml of 0.5% Ropivacaine will be given through the catheter and a continuous infusion of 0.25% Ropivacaine at the rate of 5ml per hour will be started and continued post operatively for 24hours.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 60
We include all patients between the Ages of 18-60 years undergoing proximal femur surgeries under spinal anesthesia who are having the physical status of ASA grade I and II.
Contraindications to regional anaesthesia/Known allergy to local anaesthetics Bleeding diathesis/Use of any anti-coagulants Severe kidney or liver disease Dementia that prevents proper comprehension Pregnant/Lactating females.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare Ultrasound guided continuous Erector spinae plane block versus continuous Paravertebral block for post operative analgesia using the mean maximum Visual Analog Scale score in patients undergoing in proximal fracture femur surgeries 24 hours
- Secondary Outcome Measures
Name Time Method Compare VAS score in both blocks in the first 24 hrs., the Time of rescue analgesia and total Requirement of rescue analgesic in 24 hours 24 hours
Trial Locations
- Locations (1)
VMMC And Safdarjung Hospital
🇮🇳South, DELHI, India
VMMC And Safdarjung Hospital🇮🇳South, DELHI, IndiaDr Aditya MehrotraPrincipal investigator09717268806adityameh@gmail.com