Obstetric Anesthesia and Analgesia Month Attributes in Czech Republic (OBAAMA)

This study has been completed.
Sponsor:
Collaborators:
Masaryk University
General University Hospital, Prague
Brno University Hospital
Information provided by (Responsible Party):
Jan Blaha, MD, PhD., Charles University, Czech Republic
ClinicalTrials.gov Identifier:
NCT01830218
First received: April 7, 2013
Last updated: April 11, 2013
Last verified: April 2013
  Purpose

A national survey of current practices, preferred drug and technique choices for obstetric anesthesia and analgesia in Czech Republic.


Condition Intervention
Obstetric Anesthesia Care
Procedure: Obstetric anesthesia and analgesia

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: A National Survey on Obstetric Anesthesia and Analgesia Care in Czech Republic

Further study details as provided by Charles University, Czech Republic:

Primary Outcome Measures:
  • A national survey of current practice of obstetric anesthesia and analgesia in Czech Republic [ Time Frame: Parturition period, up to 24 hours after labor ] [ Designated as safety issue: No ]
    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.


Enrollment: 1940
Study Start Date: November 2011
Study Completion Date: December 2011
Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Obstetric anesthesia and analgesia
Women in labor undergoing anesthesia care
Procedure: Obstetric anesthesia and analgesia
All anesthesia procedures during labor: labor analgesia, anesthesia for Cesarean section, anesthesia for procedures in third stage of labor

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.

  Eligibility

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Women in labor

Criteria

Inclusion Criteria:

Women in labor undergoing anesthesia care

  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01830218

Locations
Czech Republic
University Hospital Brno
Brno, Czech Republic, 625 00
Sponsors and Collaborators
Charles University, Czech Republic
Masaryk University
General University Hospital, Prague
Brno University Hospital
Investigators
Study Chair: Petr Stourac, MD, PhD. ESPAA
  More Information

Additional Information:
No publications provided

Responsible Party: Jan Blaha, MD, PhD., Chairman, ESPAA, Charles University, Czech Republic
ClinicalTrials.gov Identifier: NCT01830218     History of Changes
Other Study ID Numbers: OBAAMA 2011
Study First Received: April 7, 2013
Last Updated: April 11, 2013
Health Authority: Czech Republic: Ethics Committee

Additional relevant MeSH terms:
Anesthetics
Central Nervous System Agents
Central Nervous System Depressants
Pharmacologic Actions
Physiological Effects of Drugs
Therapeutic Uses

ClinicalTrials.gov processed this record on October 21, 2014