SAIGNEES: Phlebotomy and Lifestyle and Diet Advices vs Lifestyle and Diet Advices Only in Patients With Dysmetabolic Liversiderosis

Sponsor
Rennes University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01045525
Collaborator
Ministry of Health, France (Other)
274
5
2
71
54.8
0.8

Study Details

Study Description

Brief Summary

Insulin resistance-associated hepatic iron overload (IR-HIO), also defined as dysmetabolic iron overload syndrome or dysmetabolic liversiderosis, is a common cause or iron overload in France, mainly in middle-age patients with increased serum ferritin levels associated with normal serum transferrin saturation, and normal serum iron concentration in the absence of other known cause of increased serum ferritin levels.

Treatment includes a combination of dietary measures and physical activity to correct metabolic disorders. Phlebotomies seem to be beneficial when serum ferritin level is high.

This study aims at comparing the effect of iron depletion (by phlebotomy) plus lifestyle and diet advices versus lifestyle and diet advices alone on blood glucose level and insulin sensitivity in subjects with IR-HIO in order to assess the benefits of phlebotomies on the reduction of risk of diabetes and cardiovascular associated complications.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Phlebotomy
  • Behavioral: Lifestyle and diet advices
Phase 3

Detailed Description

Non applicable

Study Design

Study Type:
Interventional
Actual Enrollment :
274 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective Randomized Study Comparing the Effect of Phlebotomy and Lifestyle and Diet Advices vs Lifestyle and Diet Advices Only on Glycemia in Patients With Dysmetabolic Liversiderosis
Study Start Date :
Jan 1, 2010
Actual Primary Completion Date :
Jun 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Phlebotomy + lifestyle and diet advices

Procedure: Phlebotomy
From 300 to 400mL for women; From 350 to 450mL for men
Other Names:
  • Non applicable
  • Active Comparator: Lifestyle and diet advices

    Behavioral: Lifestyle and diet advices
    2 Booklets with Dietary and physical activity advices
    Other Names:
  • Non applicable
  • Outcome Measures

    Primary Outcome Measures

    1. Fasting blood glycemia (T0 of Oral Glucose Tolerance Test) [12 months]

    Secondary Outcome Measures

    1. Rate of Body mass index > 25 kg/m² [12 months]

    2. Rate of systolic blood pressure ≥ 130mmHg or diastolic blood pressure ≥ 85 mmHg or antihypertensive treatment [12 months]

    3. Rate of abdominal obesity (waist measurement ≥ 94 cm for men and ≥ 80 cm for women) [12 months]

    4. Rate of fasting triglyceridemia ≥ 1.7 mmol/L or triglyceride-lowering treatment [12 months]

    5. Rate of fasting HDL cholesterol < 1.03 mmol/L for men and < 1.29 mmol/L for women or HDL cholesterol-elevating treatment [12 months]

    6. Rate of fasting glycemia ≥ 5.6 mmol/L [12 months]

    7. HbA1c value [12 months]

    8. Quality of life estimated with SF36 form and tolerance to treatment [12 months]

    9. Insulinoresistance indexes calculated at T0 and T30 min of Oral Glucose Tolerance Test (OGTT) [12 months]

    10. Biological markers: CRP, hyaluronic acid, fibrometer [12 months]

    11. myocardial deformation [12 months]

      Two dimensional (2D) speckle tracking echocardiography (STE)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age over 18

    • Signed written informed consent

    • Ferritin ≥ 450 µg/L and ≤ 1500 µg/L

    • Hepatic iron overload proved by MRI or histological biochemical measurement (Iron hepatic concentration ≥ 50 μmol/g)

    • At least one of the following criteria :

    • Body mass index > 25 kg/m²

    • Systolic blood pressure ≥ 140mmHg or diastolic blood pressure ≥ 90 mmHg or antihypertensive treatment

    • Abdominal obesity (waist measurement ≥ 94 cm for men and ≥ 80 cm for women)

    • Fasting triglyceridemia ≥ 1.7 mmol/L or triglyceride-lowering treatment

    • Fasting HDL cholesterol < 1.03 mmol/L for men and < 1.29 mmol/L for women or HDL cholesterol-elevating treatment

    • Fasting blood glycemia ≥ 5.6 mmol/L

    Exclusion Criteria:
    • Subjects deprived of their liberty by judicial or administrative decision

    • Pregnant women

    • Other causes of increased serum ferritin levels:

    • Inflammatory syndrome (CRP >10 mg/L) or inflammatory, immune or malignant diseases

    • Hyper-hemolysis

    • Alcohol consumption more than 210 g for men and 140 g for women per week within the year before inclusion

    • Haemochromatosis established by the C282Y homozygous genotype

    • Chronic hepatic cytolysis due to : viral infection (HBV, HCV), alcohol, hyperthyroid disease, celiac disease, drug or immune hepatitis

    • Increased serum ferritin levels - cataract syndrome (familial cataract or personal history of cataract before 50 years of age)

    • Low ceruloplasmin level

    • Porphyria (cutaneous signs)

    • Contraindication of phlebotomy

    • Haemoglobin <13 g/dL for men and <12g/dL for women (threshold established by the French Blood Agency)

    • Congestive heart failure or coronary heart disease

    • Hepatic failure (TP<60%), renal failure (GFR <50mL/min) or respiratory insufficiency (chronic dyspnea)

    • Poor venous system

    • Fasting blood glycemia > 7 mmol/L or type 1 or type 2 diabetes, treated or not

    • Use of drugs known to have anti-steatotic effects : metformin, thiazolidinedione

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Clermont-Ferrand University Hospital Clermont-Ferrand France 63058
    2 La Roche Sur Yon Hospital La Roche Sur Yon France 85925
    3 Lorient Hospital Lorient France 56100
    4 Service des maladies du foie - Hôpital Pontchaillou Rennes France 35000
    5 Saint-Malo Hospital Saint-Malo France 35400

    Sponsors and Collaborators

    • Rennes University Hospital
    • Ministry of Health, France

    Investigators

    • Principal Investigator: Fabrice LAINE, MD, Rennes University Hospital
    • Study Chair: Eric BELLISSANT, MD, PhD, Rennes University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Rennes University Hospital
    ClinicalTrials.gov Identifier:
    NCT01045525
    Other Study ID Numbers:
    • EUDRACT 2009-A00831-56
    • PHRC / 09-02
    First Posted:
    Jan 11, 2010
    Last Update Posted:
    Sep 12, 2018
    Last Verified:
    Sep 1, 2018
    Keywords provided by Rennes University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 12, 2018