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Clinical Trials/NCT04691934
NCT04691934
Completed
Not Applicable

Our Anesthesia Experiences in COVID-19 Positive Patients Undergoing Cesarean Section: A Retrospective Single-center Cohort Study

Turkiye Yuksek Ihtisas Education and Research Hospital1 site in 1 country61 target enrollmentMarch 11, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
Turkiye Yuksek Ihtisas Education and Research Hospital
Enrollment
61
Locations
1
Primary Endpoint
obstetric anesthesia practices
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

At the end of 2019, a new coronavirus named COVID-19 (SARS-CoV-2), one of the lower respiratory tract samples was detected in China. The World Health Organization (WHO) declared it a global epidemic on March 11, 2020, due to the emergence of COVID-19 cases in 113 countries other than China, where the first epidemic occurred, and the spread and severity of the virus. Pregnancy increases susceptibility to respiratory complications of viral diseases.

This study aimed to retrospectively evaluate the demographic data of COVID-19 patients undergoing cesarean section, our anesthesia practices, complications, and condition of neonates, and to summarize up-to-date information on COVID-19 in obstetric anesthesia.

Detailed Description

Our study was a single-center, retrospective, and observational trial and carried out with the principles of the Declaration of Helsinki. All patient demographics and information about anesthesia were analyzed retrospectively from the patient files. All patients were operated in negative pressure operating theatres reserved for them. The whole team was equipped with Level 3 personal protective equipment (PPE) (liquid-proof apron, N-95 mask, goggles, visor, overshoes). Anesthesia was administered by 2 healthcare professionals from the anesthesia team, including an experienced anesthesiologist and an assistant anesthesia technician. A third person was kept ready outside to help in case of need.

Registry
clinicaltrials.gov
Start Date
March 11, 2020
End Date
December 25, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Turkiye Yuksek Ihtisas Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Derya Karasu, MD

Assoc Prof.

Turkiye Yuksek Ihtisas Education and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients who underwent cesarean section
  • Patients who had positive PCR nasopharyngeal swabs for COVID-19

Exclusion Criteria

  • Patients who tested negative and were clinically suspicious

Outcomes

Primary Outcomes

obstetric anesthesia practices

Time Frame: until 30 minutes after arrival in the operating room

the type of anesthesia was investigated

Secondary Outcomes

  • anesthesia complications(up to 1 hour after anesthesia)

Study Sites (1)

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