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NCT03393260 Clinical Trial

Epidemiological Characteristics and Prognosis Factors of Cancer Patients Admitted at French Emergency Departments

Emergencies Clinical Trial

— EPICANCER  

Official title:
Epidemiological Characteristics and Prognosis Factors of Cancer Patients Admitted at French Emergency Departments

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03393260
Other study ID # IRU2017
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 6, 2018
Est. completion date October 31, 2019

Study information
Verified date December 2019
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with cancer or hematological malignancy are susceptible to present acute complications linked to their disease or to their specific treatments (dyspnea, sepsis, coma, hemorrhagic syndrome). Emergency physicians are in first line when these complications arise and have to face with some complex situations in which informations about patient malignancy or prognosis may be lacking. Nowadays, there is very few epidemiological data published concerning how cancer patient use Emergency Departments (EDs) and cancer patient care delivery in the EDs.

Thus, an observational multicenter prospective cross-sectional study is conducted to study the prevalence of cancer patients admitted to French EDs, and to describe the different reasons for cancer patients to seek care in EDs with their prevalence and underscore those linked to cancer or treatment complication

Recruitment information / eligibility
Status Completed
Enrollment 1380
Est. completion date October 31, 2019
Est. primary completion date February 9, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- adult patients (age >=18 years)

- with active malignancy or a history of cancer in remission within the last 5 years

- being attended in one of the 400 French emergency centers participating in the study during the 3-day study period

Exclusion Criteria:

- opposition to participate

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Hôpital Saint Louis Paris

Sponsors (1)
Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Reasons for cancer patients to seek care in EDs 1 day
Secondary cancer location 1 day
Secondary hospitalisation rate 1 day
Secondary intensive care unit (ICU) admission 7 days
Secondary ICU mortality 7 days
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