- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02380586
Obstetric Anaesthesia And Analgesia Month Attributes - International (OBAAMA-INT)
A National Survey on Obstetric Anesthesia and Analgesia Care - International
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A one month-long project monitoring an obstetric anesthesia practices in obstetric/anesthesia departments throughout the Czech Republic.
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.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Brno, Czech Republic, 62500
- Faculty hospital Brno
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Women in labor undergoing anesthesia care
Exclusion Criteria:
- not meeting inclusion criteria
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Women in labor undergoing anesthesia care
|
All anesthesia procedures during labor: labor analgesia, anesthesia for Cesarean section, anesthesia for procedures in third stage of labor
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
A national survey of current practice of obstetric anesthesia and analgesia in Czech Republic and Slovak Republic
Time Frame: Parturition period, up to 24 hours after labor
|
Monitoring of all obstetric anesthesia procedures in peripartal period and anesthesia complications: history, form of labour analgesia, type of anesthesia for Cesarean section and anesthesia in third stage of labor.
|
Parturition period, up to 24 hours after labor
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Types of anesthesia a analgesia in peripartal period
Time Frame: Parturition period, up to 24 hours after labor
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To describe current practice a complications related to peripartal anesthesia care
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Parturition period, up to 24 hours after labor
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Complications related to obstetric anesthesia care
Time Frame: Parturition period, up to 24 hours after labor
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To describe current practice a complications related to peripartal anesthesia care
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Parturition period, up to 24 hours after labor
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Petr Štourač, MD, Ph.D, FN Brno
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MU_IBA1026
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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