Last reviewed · How we verify

NCT03836534

the Observance of Emergency Exit Treatments During the Stay of Care at the Exit of Reims Emergencies

Completed Last updated 2 March 2021
What this trial tests

trial testing adherence to treatment of patients coming out of emergencies in Patient Coming to the Emergency Department for Any Reason in 274 participants. Completed in 31 March 2019.

Timeline
11 March 2019
Primary endpoint
18 March 2019
31 March 2019

Quick facts

Lead sponsorCHU de Reims
StatusCompleted
Study typeOBSERVATIONAL
Enrollment274
Start date11 March 2019
Primary completion18 March 2019
Estimated completion31 March 2019
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

CHU de Reims — full company profile →

Who can join

18 and older, any sex, with Patient Coming to the Emergency Department for Any Reason. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators would like to include patients consulting in a Accident and Emergency Department (AED) during the permanence of care the week of March 11 to 17, 2018. The data collection would concern socio-demographic data, their consultation to the AED, the follow-up given to the consultation and would take place by telephone contact of patients within 48 hours of the consultation. why patients come to the emergency room, what are they waiting for? what are their main motivations? what do they do in emergencies, do they follow the treatments and recommendations?

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other CHU de Reims trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03836534.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing