Prospective Evaluation of the Predictive Criteria of Severity for Respiratory Infection Due to COVID-19 Virus
COPREG
1 other identifier
observational
4,734
1 country
1
Brief Summary
Emergency call centers are very solicited in epidemic situations. It is necessary to detect early Predictive Criteria of Severity in COVID respiratory infection to identify patients at risk of complication or aggravation from an emergency call center in order to adapt their orientation and their medical management.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2020
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 27, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 17, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
July 17, 2020
CompletedFirst Submitted
Initial submission to the registry
November 3, 2020
CompletedFirst Posted
Study publicly available on registry
November 4, 2020
CompletedNovember 9, 2020
November 1, 2020
3 months
November 3, 2020
November 6, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Hospitalization
Hospitalization declared by the patient 1 month after his call to the emergency call center
Month 1
Interventions
Follow-up phone call after month to detect which patient have been hospitalized
Eligibility Criteria
All patient (more than 15 years old) calling the emergency call center (15 center) for Low or High Respiratory Infection With or Without Fever and Suspected
You may qualify if:
- patient (more than 15 years old) calling the emergency call center (15 center) for Low or High Respiratory Infection With or Without Fever and Suspected to be COVID
You may not qualify if:
- unknown contact facility
- call not regulated by a practitioner from the medical emergency help team
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital of Toulouse
Toulouse, 31000, France
Study Officials
- PRINCIPAL INVESTIGATOR
Charles-Henri HOUZE-CERFON
University Hospital, Toulouse
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Month
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 3, 2020
First Posted
November 4, 2020
Study Start
April 27, 2020
Primary Completion
July 17, 2020
Study Completion
July 17, 2020
Last Updated
November 9, 2020
Record last verified: 2020-11