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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04139265
Other study ID # RC-P0079
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 6, 2019
Est. completion date September 30, 2019

Study information

Verified date October 2019
Source Lille Catholic University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Transferrin saturation coefficient and ferritinemia in diagnosis of iron deficiency


Recruitment information / eligibility

Status Completed
Enrollment 136
Est. completion date September 30, 2019
Est. primary completion date September 30, 2019
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

- = 65 years old

- Patient hospitalized in the internal medicine and geriatry service

- Patient affiliated with a social security scheme

- Patient signed an Informed consent

Exclusion Criteria:

- Risk benefit balance not in favor of iron deficiency check-up

- Patient in palliative care

Study Design


Intervention

Diagnostic Test:
biologic analysis (ferritinemia, transferrin saturation coefficient)
Each patient will follow a blood test in order to compare between ferritinemia and transferrin saturation coefficient in iron deficiency diagnosis

Locations

Country Name City State
France Saint-Philibert hospital Lomme Nord

Sponsors (1)

Lead Sponsor Collaborator
Lille Catholic University

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Agreement between Transferrin Saturation Coefficient (TSC) and ferritinemia dosage The overall agreement, assessed by kappa Cohen Day one
Secondary Prevalence of iron deficiency with and without anaemia Number of patients with iron deficiency with or without anaemia Day one
Secondary Prevalence of etiologies of iron deficiency Number of patients for each etiology Day one
Secondary Prevalence of iron deficiency in patients with anticoagulant and platelet aggregation inhibitor Day one
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