Study of the Prevalence of Iron Deficiency in Patients With Chronic Inflammatory Bowel Disease

NCT ID: NCT04123990

Last Updated: 2019-10-11

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

1100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-02

Study Completion Date

2020-03-30

Brief Summary

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Despite its known prevalence in IBD, a recent study conducted with Prof. Cacoub (unpublished) on the national health insurance database showed that iron deficiency was an under-diagnosed and under-treated co-morbidity. In chronic diseases including IBD, Transferrin Saturation Factor is only performed in approximately 10% of cases, whereas it is recommended in inflammatory situations including IBD patients (HAS 2011).

The objective of this study is therefore to obtain updated French data on the prevalence of iron deficiency in patients with IBD by applying the recommendations of ECCO and French Health High Authority (determination of ferritinemia and Transferrin Saturation Factor)

Detailed Description

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Conditions

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Intestinal Disease

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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IBD

Group Type EXPERIMENTAL

Iron status testing

Intervention Type DIAGNOSTIC_TEST

Iron status testing

Interventions

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Iron status testing

Iron status testing

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Patient, male or female, over 18 years old
* Patient present at the hospital on the day of the study
* Diagnosis of IBD on international criteria
* Patient giving written consent

Exclusion Criteria

* Protected patient: major under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision;
* pregnant, lactating or parturient woman;
* Patient hospitalized without consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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VIFORFRANCE

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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CARENFER MICI

Identifier Type: -

Identifier Source: org_study_id

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