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Ursodeoxycholic Acid in the Treatment of Duodenal Adenomas in Familial Adenomatous Polyposis (FAP) Patients
This study is ongoing, but not recruiting participants.
Study NCT00134758   Information provided by Assistance Publique - Hôpitaux de Paris
First Received: August 23, 2005   Last Updated: July 28, 2009   History of Changes

August 23, 2005
July 28, 2009
October 2004
June 2009   (final data collection date for primary outcome measure)
SPIGELMAN severity score of duodenal lesion after 2 years of follow-up [ Time Frame: Baseline, 1 and 2 years ] [ Designated as safety issue: No ]
Spigelman severity score of duodenal lesion after 2 years of follow-up.
Complete list of historical versions of study NCT00134758 on ClinicalTrials.gov Archive Site
  • Cellular proliferation (Ki 67 and PCNA) [ Time Frame: At the baseline, 1 and 2 years ] [ Designated as safety issue: No ]
  • Biliary acid profile [ Time Frame: At the baseline, 1 and 2 years ] [ Designated as safety issue: No ]
  • Compliance to the treatment [ Time Frame: Every 6 months during 2 years ] [ Designated as safety issue: No ]
  • Cellular proliferation (Ki 67 and PCNA).
  • Biliary acid profil.
  • Compliance to the treatment.
 
Ursodeoxycholic Acid in the Treatment of Duodenal Adenomas in Familial Adenomatous Polyposis (FAP) Patients
Efficiency of Ursodesoxycholic Acid in the Treatment of Duodenal Adenomas in Familial Adenomatous Polyposis Patients. URSOPAF

Malignant transformation of adenomas of the duodenum is now the leading cause of death in familial adenomatous polyposis (FAP) patients who had a restorative proctocolectomy. Ursodeoxycholic acid (UDCA) modifies the biliary acid profile and could reduce the severity of duodenal adenomas and prevent such transformation.

We designed a randomized double blinded study to evaluate the efficiency of UDCA in the treatment of duodenal adenomas. One hundred patients are planned to be included. Fifty will receive UDCA and fifty a placebo. Three duodenoscopies are planned: one before inclusion, one at the end of the first year of follow-up and one after two years of follow-up at the end of the protocol. These duodenoscopies are associated to endoscopies of the ileal reservoir performed at the time of restorative proctocolectomy and are recorded numerically. Severity of the duodenal adenomas are evaluated according to the SPIGELMAN score. Patients are seen every 6 months. Before each endoscopy, blood samples are collected for biliary acid profile analysis. Moreover, during endoscopies, duodenal fluid and ileal fluid are collected for biliary acid profile analysis, also.

At the end of the follow-up of the last patients included (nov 2008), biliary acid profile analysis will be performed and statistical analysis of the results will be performed.

Phase II, Phase III
Interventional
Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Efficacy Study
Adenomatous Polyposis Coli, Familial
  • Drug: Ursodeoxycholic acid
  • Drug: Placebo
Experimental:

Ursodeoxycholic acid during 2 years :

  • between 40 and 50 kg : 500 mg/day
  • between 51 and 75 kg : 750 mg/day
  • between 76 and 100 kg : 1000 mg/day

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
90
October 2009
June 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or female patients between 18 and 65 years of age
  • Weight less than or equal to 100 kg
  • Restorative proctocolectomy
  • Activated protein C (APC) mutation identified or more than 100 polyps on the colectomy specimen
  • SPIGELMAN score of duodenal adenoma greater than or equal to 1
  • Efficient contraceptive treatment for pre-menopausal women
  • Cooperative patient
  • Signed consent
  • Social security insurance

Exclusion Criteria:

  • SPIGELMAN score of duodenal adenoma equal to 4 with severe dysplasia
  • Hepatic disease
  • Intermesenteric desmoid tumour
  • Any severe disease
  • Daily use during the last 3 months of:

    • aspirin;
    • non-steroid anti-inflammatory drugs;
    • tamoxifen;
    • cholestyramine.
  • Pregnancy
  • Breast-feeding
Both
18 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00134758
Christophe Aucan, Department of clinical research and development
P030419, AOM 03041
Assistance Publique - Hôpitaux de Paris
Axcan Pharma
Principal Investigator: Yann RA Parc, M.D., Ph.D. Department of Digestive Surgery, Saint-Antoine Hospital, Hospital of Paris (AP/HP), Pierre et Marie Curie University, 184 rue du Faubourg Saint-Antoine, 75012 Paris, France
Assistance Publique - Hôpitaux de Paris
July 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP