Preoperative Epidural Labor Analgesia and Postoperative Pain
NCT ID: NCT03381690
Last Updated: 2019-11-22
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
222 participants
OBSERVATIONAL
2017-09-01
2018-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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Epidural (ED) emergent C-sec
Epidural labor analgesia
Epidural catheter was inserted for labor analgesia using an 18-gauge Tuohy needle and a 20 gauge epidural catheter. In our institute, for epidural labor analgesia, 10 ml bolus of 0.075% levobupivacaine mixed with fentanyl 2 μg/ml was administered and same regimen was continuously infused by patient-controlled epidural analgesia (infusion rate : 10 ml/hr, bolus : 4 ml, lockout time: 30 min).
Non-ED emergent C-sec
No interventions assigned to this group
Non-ED elective C-sec
No interventions assigned to this group
Interventions
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Epidural labor analgesia
Epidural catheter was inserted for labor analgesia using an 18-gauge Tuohy needle and a 20 gauge epidural catheter. In our institute, for epidural labor analgesia, 10 ml bolus of 0.075% levobupivacaine mixed with fentanyl 2 μg/ml was administered and same regimen was continuously infused by patient-controlled epidural analgesia (infusion rate : 10 ml/hr, bolus : 4 ml, lockout time: 30 min).
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Failure of epidural analgesia
20 Years
FEMALE
No
Sponsors
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Seoul National University Bundang Hospital
OTHER
Responsible Party
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Hyo-Seok Na
Principle investigator
Locations
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Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, South Korea
Countries
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Other Identifiers
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Csec postop pain
Identifier Type: -
Identifier Source: org_study_id
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