Landmark Guided Midline Versus Pre-procedural Ultrasound Guided Paramedian at L5S1 for Spinal Anaesthesia
- Disease/Condition
- Anaesthesia
- Drug/Device/Intervention
- Conventional landmark guided midline spinal anaesthesia
- Study type
- Interventional
- Intervention type
- procedure
- Primary sponsor
- Cork University Hospital
- Location
- Cork,Ireland, Ireland
- Phase
- N/A
- Start date
- Jul 01, 2014
- End date
- Jul 01, 2015
- Enrollment
- 120 participants
difference in number of passes between the two groups.
Spinal anesthesia is widely performed using a surface landmark based 'blind' technique.
 Multiple passes and attempts while administering spinal anesthesia are associated with a
 greater incidence of post dural-puncture headache, paraesthesia and spinal hematoma.
 
 Real time and pre-procedural neuraxial ultrasound techniques have been used to improve the
 success rate of spinal anesthesia. The use of real time ultrasound-guided spinal anesthesia
 has to date been limited to case series and case reports.Its use may be limited by the
 requirement for wide bore needles and the technical difficulties associated with simultaneous
 ultrasound scanning and needle advancement. The use of pre-procedural ultrasound has been
 shown to increase the first pass success rate for spinal anesthesia only in patients with
 difficult surface anatomic landmarks. No technique has been shown to improve the success rate
 of dural puncture when applied routinely to all patients. Routine use of pre-procedure
 ultrasound guided paramedian approach results in 50% reduction in number of passes required
 for spinal anaesthetic, from a study at Cork University Hospital (awaiting publication).
 L5-S1 is the widest interlaminar space and provides minimal contribution to overall movement
 of lumbar spine.This interspinous space might still be accessible even if the patient has
 minimal spine flexion. We also noted that spinal needle insertion via the L5-S1 interspace
 was associated with the fewest passes in the pre-procedure guided ultrasound group (although
 non-significant).
 
 We hypothesise that the routine use of pre-procedural ultrasound-guided paramedian spinal
 technique at L5S1 interspinous space will result in fewer needle passes to enter the
 subarachnoid space when compared to the conventional landmark based midline approach.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT02189681
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT02189681 through Pure Global AI's free database. This phase not specified trial is sponsored by Cork University Hospital and is currently Completed. The study focuses on Anaesthesia. Target enrollment is 120 participants.
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