Reliability of Ultrasound Assisted Epidural Analgesia in Obese and Normal Weight Parturients
NCT ID: NCT01438099
Last Updated: 2013-08-26
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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COMPLETED
300 participants
OBSERVATIONAL
2011-10-31
2013-07-31
Brief Summary
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Detailed Description
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1. to evaluate congruity between palpatory technique and ultrasound lumbar evaluation to identify the correct spinal space;
2. to compare between ultrasound evaluation and needle measure of skin-epidural space depth;
3. to compare between longitudinal and transverse ultrasound epidural space depth in obese and normal parturients;
4. to check the reduction of complications and failure rates of epidural analgesia with ultrasound assistance.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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normal subjects
parturients admitted to the labor ward who request epidural analgesia with BMI \< 30
No interventions assigned to this group
obese subjects
parturients admitted to the labor ward who request epidural analgesia with BMI \> 30
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
50 Years
FEMALE
No
Sponsors
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Università degli Studi dell'Insubria
OTHER
Responsible Party
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Paolo Severgnini
Prof.
Principal Investigators
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Paolo Severgnini, Prof.
Role: PRINCIPAL_INVESTIGATOR
Universita' degli Studi dell'Insubria, Varese, Italy
Locations
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Azienda ospedaliera ospedale Circolo e Fondazione Macchi
Varese, Varese, Italy
Countries
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Other Identifiers
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18894
Identifier Type: -
Identifier Source: org_study_id