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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04779840
Other study ID # WP-2019-06
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 20, 2020
Est. completion date January 20, 2021

Study information

Verified date February 2021
Source Weprom
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The incidence of anemia ranges from 20 to 75% depending on the type of cancer. It is often present at diagnosis and increases with specific treatments. It has an impact on overall survival and quality of life. Its origins are multiple (pure iron deficiency or functional, malnutrition, dyserythropoiesis, insufficiency renal, hemolysis, chemotherapy, radiotherapy, targeted therapies). Transfusion is the most common treatment offered in the management of anemia. The incidence of anemia and its consequences are often underestimated during cancer management. Recommendations were published in 2012. An inventory of the incidence of anemia before and after the publication of these recommendations are proposed in order to assess their impact on daily practice.


Recruitment information / eligibility

Status Completed
Enrollment 349
Est. completion date January 20, 2021
Est. primary completion date January 20, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years old, - Follow-up for cancer justifying hospitalization, - Presenting anemia defined by a hemoglobin level <11 g / dL, - Patient not having objected to the collection of his data after oral and written information. Exclusion Criteria: - patients with a hemoglobin level = 11 g / dL, - adult patients under guardianship, curatorship or deprived of liberty, - pregnancy or breast-feeding in progress at the time of hospitalization.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
anemia assessment
evaluation of anemia status

Locations

Country Name City State
France Centre Jean Bernard - Clinique Victor Hugo Le Mans

Sponsors (1)

Lead Sponsor Collaborator
Weprom

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of anemia number of patient with anemia (<11.0 g/dL) upon admission to hospital on the number of patients hospitalized over the period 2 years
Secondary Assessment of transfusion prescriptions number of transfusions performed on the number of patients hospitalized over the period 2 years
Secondary Assessment of erythropoiesis stimulating agents (EPO) prescriptions number of prescriptions for erythropoiesis stimulating agents (EPO) 2 years
Secondary Assessment of iron prescriptions number of prescriptions of iron (oral and intravenous) 2 years
Secondary Time between last transfusion and date of death Delay between the date of the last transfusion and the date of patient's death 2 years
Secondary overall survival Delay between the enrollment date and the date of patient's death 2 years
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