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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00789295
Other study ID # 29102008
Secondary ID
Status Completed
Phase N/A
First received November 10, 2008
Last updated November 10, 2008
Start date March 2004

Study information

Verified date October 2008
Source Federico II University
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of this intervention study was to evaluate in type 2 diabetic patients the effects on postprandial lipemia and other metabolic parameters (in both everyday life conditions and after a standard test meal) of two diets, one moderately rich in CHO, rich in fibre and with a low glycemic index (Mediterranean diet), and the other low in CHO and rich in MUFA (Low-CHO diet).Since adipose tissue, mainly through its lipolytic activities, is considered as having a pivotal role in the regulation of postprandial lipid metabolism, a further aim of our study was to clarify the role of adipose tissue in modulating the postprandial lipid response induced by the two dietary approaches by evaluating the activities of lipoprotein lipase (LPL) and hormone-sensitive lipase (HSL).


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria:

- Type 2 diabetes

- Stable metabolic control (HbA1c<8.0%) on diet or diet alone or diet+metformin

- BMI<30 kg/m2 and body weight stable during the last six months.

- Both sexes; only post-menopausal women.

- Normal fasting lipid levels

- No use of hypolipidemic drugs

Exclusion Criteria:

- Patient with renal (serum creatinine >1.5 mg/dl) or hepatic (serum transaminases >three times upper normal values) impairment.

- Patients with history of cardiovascular disease.

- Pre-menopausal women.

- Any other acute or chronic degenerative disease.

- Anemia (Hb<12 g/dl).

- Uncontrolled blood pressure.

- Use of any drugs able to interfere with the study medications

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Mediterranean diet and Low-Carbohydrates diet
The Mediterranean diet: relatively rich in Carbohydrate(52% of the total daily energy intake), rich in dietary fibre (28g/1000 kcal both of soluble and unsoluble types) and with a low glycemic index (51%) versus Low-carbohydrates diet : diet rich in MUFA (23%), relatively low in CHO (45%), low in dietary fibre (8g/1000 kcal) and with a relatively high glycemic index (87%)for 4 weeks

Locations

Country Name City State
Italy Department of Clinical and Experimental Medicine, Federico II University Hospital, Naples

Sponsors (1)

Lead Sponsor Collaborator
Federico II University

Country where clinical trial is conducted

Italy, 

References & Publications (3)

Lairon D, Play B, Jourdheuil-Rahmani D. Digestible and indigestible carbohydrates: interactions with postprandial lipid metabolism. J Nutr Biochem. 2007 Apr;18(4):217-27. Epub 2006 Oct 31. Review. — View Citation

Lopez-Miranda J, Williams C, Lairon D. Dietary, physiological, genetic and pathological influences on postprandial lipid metabolism. Br J Nutr. 2007 Sep;98(3):458-73. Review. — View Citation

Rivellese AA, De Natale C, Di Marino L, Patti L, Iovine C, Coppola S, Del Prato S, Riccardi G, Annuzzi G. Exogenous and endogenous postprandial lipid abnormalities in type 2 diabetic patients with optimal blood glucose control and optimal fasting triglyceride levels. J Clin Endocrinol Metab. 2004 May;89(5):2153-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Postprandial response triglyceride of chylomicrons and large VLDL 4 weeks
Secondary Blood glucose and insulin response to test meal 4 weeks No
Secondary Lipolytic activities 4 weeks No
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