Retrospective Study on the Incidence and Management of Anemia in Oncology

NCT ID: NCT04779840

Last Updated: 2021-03-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

349 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-20

Study Completion Date

2021-01-20

Brief Summary

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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.

Detailed Description

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Conditions

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Anemia Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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period 2011

anemia assessment

Intervention Type OTHER

evaluation of anemia status

period 2018

anemia assessment

Intervention Type OTHER

evaluation of anemia status

Interventions

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anemia assessment

evaluation of anemia status

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Weprom

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Katell LE DÛ, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Jean Bernard/Clinique Victor Hugo - LE MANS

Locations

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Centre Jean Bernard - Clinique Victor Hugo

Le Mans, , France

Site Status

Countries

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France

Other Identifiers

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WP-2019-06

Identifier Type: -

Identifier Source: org_study_id

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