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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04758286
Other study ID # RC2-2-2021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date February 11, 2021

Study information

Verified date February 2021
Source Benha University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A protocol applied during anesthesia and surgical interventions for patients with emergency surgical conditions during the era of COVID-19 disease


Description:

All COVID-19 patients who were admitted to emergency departments presenting with emergency surgical conditions were evaluated for assurance of having COVID-19 disease. Then, the appropriate anesthetic procedure was applied and the appropriate surgical intervention was performed.


Recruitment information / eligibility

Status Completed
Enrollment 209
Est. completion date February 11, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Assured diagnosis of COVID-19 by RT-PCR Exclusion Criteria: - No

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Emergency surgical procedures
COVID-19 patients who had presented to the Emergency Department were evaluated for their emergency surgical conditions and were managed appropriately

Locations

Country Name City State
Egypt Faculty of Medicine Banha Qalubia

Sponsors (2)

Lead Sponsor Collaborator
Benha University Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Questionnaire This questionnaire was designed to assess the satisfaction of the anesthetist in-charge and the surgeon by the applied protocol to manage COVID-19 patients Up to two days
Secondary Physiologic assessment estimation of systolic and diastolic blood pressures of patients during and after surgery Up to one day
Secondary Surgical follow-up Postoperative assessment of wounds and drainage tube, if any, and to determine the success of the procedure or the development of complications Up to 10 days
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