Obstetric Anesthesia and Analgesia Month Attributes in Czech Republic

Obstetric Anesthesia Care Clinical Trial

— OBAAMA  

Official title:

A National Survey on Obstetric Anesthesia and Analgesia Care in Czech Republic

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01830218
• Other study ID #: OBAAMA 2011
• Status: Completed
• Phase: N/A
• First received: April 7, 2013
• Last updated: April 11, 2013
• Start date: November 2011
• Est. completion date: December 2011

Study information

• Verified date: April 2013
• Source: Charles University, Czech Republic
• Contact: n/a
• Is FDA regulated: No
• Health authority: Czech Republic: Ethics Committee
• Study type: Observational

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1940
• Est. completion date: December 2011
• Est. primary completion date: December 2011
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

Women in labor undergoing anesthesia care

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

• Obstetric Anesthesia Care

Intervention

Procedure:
• Obstetric anesthesia and analgesia
All anesthesia procedures during labor: labor analgesia, anesthesia for Cesarean section, anesthesia for procedures in third stage of labor

Locations

Country	Name	City	State
Czech Republic	University Hospital Brno	Brno

Sponsors (4)

Lead Sponsor	Collaborator
Charles University, Czech Republic	Brno University Hospital, General University Hospital, Prague, Masaryk University

Country where clinical trial is conducted

Czech Republic, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	A national survey of current practice of obstetric anesthesia and analgesia in Czech Republic	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	No

External Links

•   Study webpage