Obstetric Anesthesia and Analgesia Month Attributes in Czech Republic
NCT ID: NCT01830218
Last Updated: 2013-04-12
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
1940 participants
OBSERVATIONAL
2011-11-30
2011-12-31
Brief Summary
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Detailed Description
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Electronic Case Report Form (eCRF) is used to collect data on all obstetric anesthesia procedures in peripartal period and obstetric and anesthesia complications. All consecutive cases in each participating center during the study period are recorded. Each record is related to parturient and contains the following sections: history, form of labour analgesia, type of anesthesia for Cesarean section and anesthesia in third stage of labor.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Obstetric anesthesia and analgesia
Women in labor undergoing anesthesia care
Obstetric anesthesia and analgesia
All anesthesia procedures during labor: labor analgesia, anesthesia for Cesarean section, anesthesia for procedures in third stage of labor
Interventions
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Obstetric anesthesia and analgesia
All anesthesia procedures during labor: labor analgesia, anesthesia for Cesarean section, anesthesia for procedures in third stage of labor
Eligibility Criteria
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Inclusion Criteria
FEMALE
No
Sponsors
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Masaryk University
OTHER
General University Hospital, Prague
OTHER
Brno University Hospital
OTHER
Charles University, Czech Republic
OTHER
Responsible Party
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Jan Blaha, MD, PhD.
Chairman, ESPAA
Principal Investigators
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Petr Stourac, MD, PhD.
Role: STUDY_CHAIR
ESPAA
Locations
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University Hospital Brno
Brno, , Czechia
Countries
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Related Links
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Study webpage
Other Identifiers
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OBAAMA 2011
Identifier Type: -
Identifier Source: org_study_id
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