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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02380586
Other study ID # MU_IBA1026
Secondary ID
Status Completed
Phase N/A
First received February 28, 2015
Last updated July 22, 2016
Start date November 2015
Est. completion date December 2015

Study information

Verified date July 2016
Source Brno University Hospital
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 and Slovak 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 3040
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Female
Age group 16 Years to 70 Years
Eligibility Inclusion Criteria:

- Women in labor undergoing anesthesia care

Exclusion Criteria:

- not meeting inclusion criteria

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


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 Faculty Hospital Brno Brno

Sponsors (5)

Lead Sponsor Collaborator
Brno University Hospital Charles University, Czech Republic, Czech society of anesthesiology, resuscitation a intensive care - CLS JEP, General University Hospital, Prague, Masaryk University

Country where clinical trial is conducted

Czech Republic, 

Outcome

Type Measure Description Time frame Safety issue
Other Complications related to obstetric anesthesia care To describe current practice a complications related to peripartal anesthesia care Parturition period, up to 24 hours after labor Yes
Primary A national survey of current practice of obstetric anesthesia and analgesia in Czech Republic and Slovak 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
Secondary Types of anesthesia a analgesia in peripartal period To describe current practice a complications related to peripartal anesthesia care Parturition period, up to 24 hours after labor No
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