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

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

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01045525
Acronym
SAIGNEES
Enrollment
274
Registered
2010-01-11
Start date
2010-01-31
Completion date
2015-12-31
Last updated
2023-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iron Overload, Liver Cirrhosis

Keywords

Phlebotomy, Dysmetabolic liversiderosis, Hepatic Iron overload

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.

Detailed description

Non applicable

Interventions

PROCEDUREPhlebotomy

From 300 to 400mL for women; From 350 to 450mL for men

BEHAVIORALLifestyle and diet advices

2 Booklets with Dietary and physical activity advices

Sponsors

Ministry of Health, France
CollaboratorOTHER_GOV
Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frame
Fasting blood glycemia (T0 of Oral Glucose Tolerance Test)12 months

Secondary

MeasureTime frameDescription
Rate of systolic blood pressure ≥ 130mmHg or diastolic blood pressure ≥ 85 mmHg or antihypertensive treatment12 months
Rate of abdominal obesity (waist measurement ≥ 94 cm for men and ≥ 80 cm for women)12 months
Rate of fasting triglyceridemia ≥ 1.7 mmol/L or triglyceride-lowering treatment12 months
Rate of fasting HDL cholesterol < 1.03 mmol/L for men and < 1.29 mmol/L for women or HDL cholesterol-elevating treatment12 months
Rate of fasting glycemia ≥ 5.6 mmol/L12 months
Rate of Body mass index > 25 kg/m²12 months
Quality of life estimated with SF36 form and tolerance to treatment12 months
Insulinoresistance indexes calculated at T0 and T30 min of Oral Glucose Tolerance Test (OGTT)12 months
Biological markers: CRP, hyaluronic acid, fibrometer12 months
myocardial deformation12 monthsTwo dimensional (2D) speckle tracking echocardiography (STE)
HbA1c value12 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026