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Effects of Docosahexaenoic Acid (DHA) on Cardiovascular Disease on Diabetic Patients

Not Applicable
Completed
Conditions
Type 2 Diabetes
Interventions
Dietary Supplement: First period DHA
Dietary Supplement: Second period DHA
Registration Number
NCT01150292
Lead Sponsor
Hospices Civils de Lyon
Brief Summary

Aim: to determine the effects of DHA supplementation:

* on the platelet function through their aggregation and the pathway of arachidonic acid metabolism

* on redox status on cells and plasma

* on inflammation in 16 type 2 diabetic patients in a cross-over study comparing DHA (400 mg/day for 2 weeks) vs Sunflower oil (placebo). Each period is separated by a wash-out period of 6 to 9 weeks.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
16
Inclusion Criteria
  • woman
  • Type 2 diabetes
  • Menopausal or aged between 55 and 75 years old
  • Recent HbA1c between 6.5-10%
  • Oral anti-diabetic drugs or insulin therapy
  • Hypertension or antihypertensive drug
Exclusion Criteria
  • Tobacco
  • Excessive drinking
  • Post-menopausal hormonal treatment
  • Treatment by acetylsalicylic acid, clopidogrel, gliclazide, ticlopidine, NSAID
  • Secondary cardiovascular prevention
  • antioxidant using
  • Fish intake >2 times a week
  • Anemia <10g/L
  • Thrombopenia <110g/L
  • Creatinine clearance <30 ml/min and/or proteinuria >1g/L

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
DHA - Sunflower oilFirst period DHA400 mg DHA supplementation by day for 2 weeks then placebo for 2 weeks after a wash out period of 6 to 9 weeks
Sunflower oil - DHASecond period DHAPlacebo during 2 weeks then 400 mg DHA supplementation by day for 2 weeks after a wash out period for 6 to 9 weeks
Primary Outcome Measures
NameTimeMethod
Platelet function induced by collagen4 blood sampling in 10 to 13 weeks

4 blood sampling are made during the time of study which expand from 10 weeks (washout period of 6 weeks) to 13 weeks (washout period of 9 weeks):

* first at the beginning of the first period

* second at the end of the period (2 weeks after beginning)

* third at the beginning of the second period

* fourth at the end of the period (2 weeks after beginning)

Secondary Outcome Measures
NameTimeMethod
Evaluation of cellular and plasmatic redox status4 blood sampling in 10 to 13 weeks

blood sampling are made during the time of study which expand from 10 weeks (washout period of 6 weeks) to 13 weeks (washout period of 9 weeks):

first at the beginning of the first period second at the end of the period (2 weeks after beginning) third at the beginning of the second period fourth at the end of the period (2 weeks after beginning)

Trial Locations

Locations (2)

Centre de Recherche en Nutrition Humaine (CRNH) Rhône-Alpes

🇫🇷

Pierre-benite, France

Hospices Civils de Lyon

🇫🇷

Bron, France

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