Sonographic Predictors of Difficult Epidural Placement.
NCT ID: NCT05893264
Last Updated: 2025-03-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2023-08-14
2023-08-14
Brief Summary
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The present study aims to identify predictors of difficult epidural placement in patients undergoing surgery.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Epidural placement
All patients undergoing epidural placement will be enrolled.
Data collection
Several data will be collected such as:
Age, weight, height, gender, previous spine surgery, skoliosis (Y/N), palpable spinous process (Y/N), experience in years of anesthesiologist, spine level of epidural placement
and the following sonographic parameters at the level of epidural placement: skin-spinous process distance (cm), skin-transversous process distance (cm), erector spinae plane distance (cm), superior to inferior spinous process distance (cm)
Interventions
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Data collection
Several data will be collected such as:
Age, weight, height, gender, previous spine surgery, skoliosis (Y/N), palpable spinous process (Y/N), experience in years of anesthesiologist, spine level of epidural placement
and the following sonographic parameters at the level of epidural placement: skin-spinous process distance (cm), skin-transversous process distance (cm), erector spinae plane distance (cm), superior to inferior spinous process distance (cm)
Eligibility Criteria
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Inclusion Criteria
* Age \> 18 years
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of Padova
OTHER
Responsible Party
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Alessandro De Cassai
Principal Investigator
Locations
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University Hospital of Padova
Padua, Veneto, Italy
Countries
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Other Identifiers
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PREC-EPI
Identifier Type: -
Identifier Source: org_study_id
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