ClinicalTrials.gg
CompletedNCT03393260EPICANCERUpdated Jan 7, 2020

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

An observational study in Cancer Patients and Emergencies, sponsored by Assistance Publique - Hôpitaux de Paris. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-01-07.

Primary conditionNeoplasmsRegistry: EmergenciesReclassifiedWhy we changed it
Registry
Emergencies — the first condition term the registry derived for this study.
ClinicalTrials.gg
Neoplasms
Why
  1. Emergencies describes something many studies share rather than a condition a study is about.
  2. The study's listed conditions name Neoplasms.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Assistance Publique - Hôpitaux de Paris · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
1,380
Ages
18 Years and older
Sex
All
01

Study 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

02

Conditions studied

  • Cancer Patients
  • Emergencies

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Keywords

  • cancer
  • emergency departments (ED)
03

In context

Neoplasms Reclassified

10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.

This study's enrollment of 1,380 is above the median of 200 across 2,638 observational studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Assistance Publique - Hôpitaux de Paris is the lead sponsor of 3,592 studies on the registry; 1,033 are open to participants now.

Compared within Neoplasms, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Emergencies. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients of 18 years or more with active malignancy or in remission for less than 5 years and being attended in one of the 400 French emergency centers participating in the study during 3 consecutive days will be enrolled

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • adult patients (age >=18 years)
  • with active 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

Exclusion Criteria:

  • opposition to participate
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
1,380 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Reasons for cancer patients to seek care in EDs

    Time frame: 1 day

Secondary outcomes

  1. cancer location

    Time frame: 1 day

  2. hospitalisation rate

    Time frame: 1 day

  3. intensive care unit (ICU) admission

    Time frame: 7 days

  4. ICU mortality

    Time frame: 7 days

07

Study locations

1 site
  • Hôpital Saint Louis
    Paris, 75010, France
08

References and documents

Publications

  • Peyrony O, Fontaine JP, Trabattoni E, Nakad L, Charreyre S, Picaud A, Bosc J, Viglino D, Jacquin L, Laribi S, Pereira L, Thiriez S, Paquet AL, Tanneau A, Azoulay E, Chevret S, Initiatives de Recherche Aux Urgences Iru-Sfmu Research Group. Cancer Patients' Prehospital Emergency Care: Post Hoc Analysis from the French Prospective Multicenter Study EPICANCER. J Clin Med. 2021 Mar 9;10(5):1145. doi: 10.3390/jcm10051145. PubMed 33803366 ↗
09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Feb 2018 to primary completion in Feb 2018, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 20, 2017
First posted
Jan 8, 2018
StartActual
Feb 6, 2018
Primary completionActual
Feb 9, 2018
CompletionActual
Oct 31, 2019
Last update
Jan 7, 2020
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 7, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03393260
Responsible party
Sponsor
First posted
Jan 8, 2018
Start date
Feb 6, 2018
Primary completion
Feb 9, 2018
Completion
Oct 31, 2019
Last update
Jan 7, 2020

Study contacts

Olivier Peyrony, MD
principal investigator · Assistance Publique - Hôpitaux de Paris

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2019. You cannot join it, but the record below documents what was studied.

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