Anesthesia Clinical Trial
Official title:
A Randomized Controlled Trial of Pre-procedural Ultrasound Techniques Versus the Conventional Landmark Technique of Spinal Anesthesia in Elderly Patients
| NCT number | NCT02658058 |
| Other study ID # | ANES.SS.13 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | November 2015 |
| Est. completion date | January 2018 |
| Verified date | January 2019 |
| Source | American University of Beirut Medical Center |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Traditionally, spinal anesthesia is performed using the palpation of bony landmark to identify the level and point of entry of the spinal needle. Recently, ultrasound imaging has become an increasingly popular procedure among anesthesiologists to guide neuraxial blockade. Most of the studies on pre-procedural ultrasound-guided neuraxial techniques are limited to a midline approach using a transverse median views. The parasagittal oblique view consistently offers better ultrasound view of the neuraxis compared to the transverse median view. However, it is still not evident whether these superior parasagittal oblique views will lead to an easier paramedian needle insertion. In the literature, there are no studies directly comparing the US-guided paramedian approach using the parasagittal oblique (PSO) view, the US-guided midline approach using the transverse median view, and the conventional landmark midline approach to perform spinal anesthesia in the elderly patients, in particular for the teaching of novice anesthesia residents.
| Status | Completed |
| Enrollment | 180 |
| Est. completion date | January 2018 |
| Est. primary completion date | January 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 60 Years and older |
| Eligibility |
Inclusion Criteria: - Patients scheduled for surgery amenable to spinal anesthesia, aged more than 60 years, with American Society of Anesthesiologists physical status 1 to 4. Exclusion Criteria: - Patients who are unable to give consent, refuse spinal anesthesia, have spinal abnormalities (including scoliosis and previous spine operations with instrumentation) or have contraindications to spinal anesthesia, including allergy to local anesthetics or a bleeding diathesis |
| Country | Name | City | State |
|---|---|---|---|
| Lebanon | American University of Beirut Medical center | Beirut |
| Lead Sponsor | Collaborator |
|---|---|
| American University of Beirut Medical Center |
Lebanon,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Rate of successful dural puncture on the first needle insertion attempt | Rate of successful dural puncture on the first needle insertion attempt which is defined as the percentage of successful dural puncture on the first introducer needle advancement through skin; each skin puncture by introducer is considered as a needle insertion attempt. | up to 5 minutes from the start of insertion of the introducer of the spinal needle | |
| Secondary | overall success rate in every technique | Overall success rate in every technique is defined as percentage of successful spinal anesthesia as evidenced by CSF flow through the spinal needle before spinal drug injection and a sensory block level >T10 15min after injection of spinal drug. | 60 minutes from the start of insertion of introducer of the spinal needle | |
| Secondary | Number of introducer needle insertion attempts | Number of introducer needle insertion attempts is defined as the number of times the introducer needle was withdrawn from the skin and reinserted. | 45 minutes from the start of insertion of introducer of the spinal needle | |
| Secondary | spinal procedure time | In groups US, period beginning when probe is first placed on patient's back and ending when examination is complete. In group LM, period beginning when patient's back is palpated first and ending when examination is complete. |
60 minutes | |
| Secondary | patient satisfaction | Patient satisfaction will be scored as following: Very good Good Satisfactory Unpleasant Very unpleasant |
5 min after completion of administration of SA: | |
| Secondary | Number of spinal needle redirections | Spinal needle redirected without complete withdrawal of the introducer of the spinal needle from skin | 45 minutes |
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