The goal of this clinical trial is to find out whether height-based dosing of spinal anaesthesia provides better hemodynamic stability and anesthetic outcome than conventional fixed dosing in elderly patients undergoing lower limb orthopaedic surgery.The main questions this study aims to answer are: 1. Does height-based spinal anaesthetic dosing reduce the risk of hypotension and bradycardia during surgery as compared to conventional fixed dosing? 2. Does it improve anaesthetic outcomes, such as the onset and duration of sensory and motor block?
Age range
60 Years – 80 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
HYPOTENSION
Timeframe: Subsequent to the administration of spinal anaesthesia till the end of sensory and motor blockade
BRADYCARDIA
Timeframe: Subsequent to the administration of spinal anaesthesia till the end of sensory and motor blockade
ONSET OF SENSORY BLOCK
Timeframe: Subsequent to the administration of spinal anaesthesia till the attainment of sensory blockade
DURATION OF SENSORY BLOCK
Timeframe: Subsequent to the administration of spinal anaesthesia till the end of sensory blockade
ONSET OF MOTOR BLOCK
Timeframe: Subsequent to the administration of spinal anaesthesia till the attainment of motor blockade
DURATION OF MOTOR BLOCK
Timeframe: Subsequent to the administration of spinal anaesthesia till the end of motor blockade