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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04912791
Other study ID # MU_IBA2021
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date February 1, 2022

Study information

Verified date October 2021
Source Brno University Hospital
Contact Petr Stourac, prof.MD., Ph.D.
Phone 532234404
Email stourac.petr@fnbrno.cz
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A national survey of current practices, preferred drug and technique choices for obstetric anesthesia and analgesia and to evaluate the impact of COVID-19 pandemic on 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 and Slovak 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 Not yet recruiting
Enrollment 5000
Est. completion date February 1, 2022
Est. primary completion date January 31, 2022
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


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
Czechia Brno University Hospital Brno South Moravian Region

Sponsors (4)

Lead Sponsor Collaborator
Brno University Hospital Czech Society of Anaesthesiology, resuscitation and intensive care (CSARIM), Institute of Biostatistics and Analyses, Masaryk University Brno, Medical Faculty of Masaryk University, Brno, Czech Republic

Country where clinical trial is conducted

Czechia, 

Outcome

Type Measure Description Time frame Safety issue
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
Secondary Types of anesthesia a analgesia in peripartal period To describe current practice related to peripartal anesthesia care Parturition period, up to 24 hours after labor
Secondary 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
See also
  Status Clinical Trial Phase
Completed NCT02380586 - Obstetric Anaesthesia And Analgesia Month Attributes - International N/A
Completed NCT01830218 - Obstetric Anesthesia and Analgesia Month Attributes in Czech Republic N/A