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Completed

NCT Number: NCT01572818

Effects of Phlebotomy on Insulin Sensitivity in Insulin Resistance-associated Hepatic Iron Overload Patients

The purpose of this study is to evaluate efficacy of phlebotomy on insulin sensitivity as evaluated by euglycemic-hyperinsulinic clamp in insulin resistance-associated hepatic iron overload patients.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHU, Nantes, France

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About this study

The main objective of this study is to evaluate in patients with HSD effects of treatment with phlebotomy rules with lifestyle and dietary rules versus lifestyle modifications alone on peripheral insulin resistance (assessed by hyperinsulinemic clamp).

Secondary objectives are:

  • to study in all patients with HSD the relationship between the amount of iron intrahepatic and degree of peripheral insulin resistance and liver before therapeutic intervention.
  • to study and compare the effects of phlebotomy treatment versus no treatment on:
  • Plasma levels of adipocytokines,
  • Plasma concentrations of inflammatory markers and markers of insulin resistance,
  • The serum ferritin,
  • The post-hepatic clearance of insulin,
  • The surface of the abdominal visceral fat and subcutaneous abdominal.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18 and 70 years
  • Ferritin between 450 and 1000 µg/L
  • Hepatic iron overload proved by MRI (CHF >36 µmol/g)
  • Body mass index > 25 kg/m²
  • Fasting glycemia <1,26 g/L
  • HbA1c < 6,5%
  • Signed written and informed consent

Exclusion criteria

  • Other causes of hyperferritinemia:
  • Inflammatory syndrome (CRP >10 mg/L) or inflammatory, immune or malignant diseases
  • Hyperferritinemia-cataract syndrome (familial cataract or personal history of cataract before 50 years old)
  • Low ceruloplasmin level
  • Porphyria (cutaneous signs)
  • Haemochromatosis established by the genotype (C282Y homozygous or C282Y/H63D coumpound heterozygous genotypes)
  • Contraindication of phlebotomy
  • Haemoglobin <13,5 g/dL (threshold established by the Etablissement Français du Sang)
  • Heart failure or coronary heart diseases
  • Hepatic failure, renal (GFR <50mL/min) or respiratory insufficiency (chronic dyspnea)
  • Poor venous system
  • Viral, immune, genetic, vascular, malignant or toxic chronic hepatic disease
  • Alcohol consumption more than 21 doses per week during 5 years or more
  • Type 1 or type 2 diabetes
  • Oral anti-diabetic, corticoids or immune suppressor drugs
  • Hepatic severe disease
  • Claustrophobia, having a pace-maker or intracerebral clips
  • Subjects deprived of their liberty by judicial or administrative decision, subjects that are not affiliated to social security or topics exclusion period of a previous study

Treatment and study plan

Phlebotomy

Procedure

7 ml/kg without exceeding 500 mL

Other names: Non applicable.

dietary and lifestyle counseling

Behavioral

dietary and lifestyle counseling

Other names: Non applicable.

Primary outcomes

  1. Glucose Infusion Rate by euglycemic-hyperinsulinic clamp

    Time frame: 6 months

Secondary outcomes

  1. hepatic parameters

    Time frame: 6 months

  2. inflammation markers

    Time frame: 6 months

    IL-6, TNF alpha, CRP

  3. Adipokins markers

    Time frame: 6 months

    adiponectin, PAI1, leptin

  4. SHBG

    Time frame: 6 months

  5. HOMA-IR

    Time frame: 6 months

  6. Hepatic iron overload (MRI)

    Time frame: 6 months

    transaminase (ALT, AST), gamma GT

  7. Abdominal and sub-cutaneous fat surface (MRI)

    Time frame: 6 months

  8. iron parameters

    Time frame: at 6 months

    serum iron, ferritin, saturation of transferrin

  9. lipid profile

    Time frame: at 6 months

    HDL-c, LDL-c, triglycerides

Sponsors and collaborators

Lead sponsor

Rennes University Hospital

Other

Registry information

Acronym: SAINPOS

Important dates

Study start
2010
Primary completion
2015
Study completion
2015
First posted
Apr 6, 2012
Registry last updated
Jun 15, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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