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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01428843
Other study ID # GETAID 2009-2
Secondary ID 2009-011316-38
Status Terminated
Phase Phase 3
First received August 30, 2011
Last updated June 21, 2015
Start date January 2011
Est. completion date December 2014

Study information

Verified date June 2015
Source Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

Anemia is the the most frequently extradigestive symptom for Inflammatory Bowel Disease. This is due to iron deficiency and inflammation.

Most of treatments aim to control inflammation using anti-TNF alpha therapy which should theorically reduce anemia.

The aim of the study is to show that perfusion of iron associated to anti-TNF therapy should reduce anemia and improve quality of life of patients.


Recruitment information / eligibility

Status Terminated
Enrollment 60
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age greater than 18 years

- Crohn's disease or Ulcerative Colitis defined according to the usual endoscopic, histological, and radiological criteria

- Under anti-TNF therapy or indication for starting an anti-TNF therapy

- Anemia defined according to World Health Organization (Hemoglobin under 13g/dl for man and Hemoglobin under 12g/dl for woman)

- Iron deficiency anemia defined as:

- Ferritinemia under 100 if C-Reactive Protein under normal value OR - Ferritinemia between 30 and 100 if C-Reactive Protein above normal value

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Intervention

Drug:
FERRISAT
A single infusion of 50 mg/ml of Ferrisat during inclusion visit.
PLACEBO
A single infusion of Glucose 5% solution during inclusion visit

Locations

Country Name City State
France Chu Amiens Amiens
France CHU CAEN Caen
France Chu Clermont-Ferrand Clermont-ferrand
France Hopital Beaujon Clichy
France Hopital Bicetre Le Kremlin Bicetre
France CHRU Lille Lille
France Chu Marseille - Hopital Nord Marseille
France Chu Nantes Nantes
France Hopital Cochin Paris
France Hopital Saint Louis Paris
France Hopital St Antoine Paris
France CHU Bordeaux - Pessac Pessac
France CHU LYON Pierre Benite
France Chu Rennes Rennes
France Chu Rouen Rouen
France Chu Saint Etienne St Etienne
France Chu Toulouse Toulouse
France Chu Tours Tours

Sponsors (1)

Lead Sponsor Collaborator
Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives

Country where clinical trial is conducted

France, 

References & Publications (6)

Gasche C, Berstad A, Befrits R, Beglinger C, Dignass A, Erichsen K, Gomollon F, Hjortswang H, Koutroubakis I, Kulnigg S, Oldenburg B, Rampton D, Schroeder O, Stein J, Travis S, Van Assche G. Guidelines on the diagnosis and management of iron deficiency an — View Citation

Gisbert JP, Gomollón F. Common misconceptions in the diagnosis and management of anemia in inflammatory bowel disease. Am J Gastroenterol. 2008 May;103(5):1299-307. doi: 10.1111/j.1572-0241.2008.01846.x. Review. — View Citation

Oldenburg B, Koningsberger JC, Van Berge Henegouwen GP, Van Asbeck BS, Marx JJ. Iron and inflammatory bowel disease. Aliment Pharmacol Ther. 2001 Apr;15(4):429-38. Review. — View Citation

Ormerod TP. Observations on the incidence and cause of anaemia in ulcerative colitis. Gut. 1967 Apr;8(2):107-14. — View Citation

Vijverman A, Piront P, Belaiche J, Louis E. Evolution of the prevalence and characteristics of anemia in inflammatory bowel diseases between 1993 and 2003. Acta Gastroenterol Belg. 2006 Jan-Mar;69(1):1-4. — View Citation

Wilson A, Reyes E, Ofman J. Prevalence and outcomes of anemia in inflammatory bowel disease: a systematic review of the literature. Am J Med. 2004 Apr 5;116 Suppl 7A:44S-49S. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Level of hemoglobin Efficacy of one-shot perfusion of Ferrisat (Iron supplementation) 6 weeks after inclusion No
Secondary Tolerance of Ferrisat At Inclusion Yes
Secondary Improvement of quality of life 6 weeks after perfusion No
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