Epidural Analgesia Versus IV Meperidine for Labor Pain Control
NCT ID: NCT00296751
Last Updated: 2010-07-01
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
NA
60 participants
INTERVENTIONAL
2006-03-31
2006-12-31
Brief Summary
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Detailed Description
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* Inclusion criteria : all parturients requiring pain relief will choose between systemic or epidural analgesia.
* Exclusion Criteria: all parturients with cardiac disease, neurological disease, endocrine disease, diabetes, hypertension or any parturients being treated with medications that might effect the cardiovascular autonomic system.
* Method: A 10 minute recording of a 3 lead ECG will be performed during the second stage of the delivery (3-7 CM opening).
the parturient will be lying on her left side for that period.
* 30 minutes after administration of either epidural or systemic Meperidine for pain relief, a second recording of maternal ECG will take place for 10 minutes.
* estimated duration of the procedure about one hour per woman.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
NONE
Interventions
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ECG recording
Epidural catheter insertion
Intravenous meperidine injection
Epidural Bupivacaine and fentanyl injection
Eligibility Criteria
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Exclusion Criteria
20 Years
40 Years
FEMALE
Yes
Sponsors
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Rambam Health Care Campus
OTHER
Principal Investigators
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Amir Weissman, MD
Role: STUDY_DIRECTOR
Rambam Health Care Campus
Olga Torchov, MD
Role: PRINCIPAL_INVESTIGATOR
Rambam Health Care Campus
Locations
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Rambam - health care campus
Haifa, , Israel
Countries
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Other Identifiers
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epiduralCTIL
Identifier Type: -
Identifier Source: org_study_id
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