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Completed

NCT Number: NCT02380586

Obstetric Anaesthesia And Analgesia Month Attributes - International

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

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Key information

Conditions

Obstetric Anesthesia Care

Age range

16 year–70 year

Sex eligibility

Female

Study type

Observational

Primary location

Faculty Hospital Brno

Brno, Czech Republic, 62500, Czechia

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women in labor undergoing anesthesia care

Exclusion criteria

  • not meeting inclusion criteria

Treatment and study plan

Obstetric anesthesia and analgesia

Procedure

All anesthesia procedures during labor: labor analgesia, anesthesia for Cesarean section, anesthesia for procedures in third stage of labor

Primary outcomes

  1. 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.

Secondary outcomes

  1. Types of anesthesia a analgesia in peripartal period

    Time frame: Parturition period, up to 24 hours after labor

    To describe current practice a complications related to peripartal anesthesia care

Other outcomes

  1. Complications related to obstetric anesthesia care

    Time frame: Parturition period, up to 24 hours after labor

    To describe current practice a complications related to peripartal anesthesia care

Sponsors and collaborators

Lead sponsor

Brno University Hospital

Other

Collaborators

  • Charles University, Czech Republic
  • Czech society of anesthesiology, resuscitation a intensive care - ČLS JEP
  • General University Hospital, Prague
  • Masaryk University

Registry information

Official study title

A National Survey on Obstetric Anesthesia and Analgesia Care - International

Acronym: OBAAMA-INT

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Mar 5, 2015
Registry last updated
Jul 26, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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