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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03047668
Other study ID # POLYPHEM
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2013
Est. completion date December 2020

Study information

Verified date July 2020
Source German Institute of Human Nutrition
Contact Stefan Kabisch, Dr. med.
Phone 030 450 514 429
Email stefan.kabisch@dife.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Basic treatment of type 2 diabetes should focus on diet, physical activity and lifestyle. Nevertheless, in early and late stage of T2DM, lifestyle intervention is mostly substituted by pharmacological intervention, although lifestyle modification and dietary treatment would be favourable.

The researchers therefore investigate dietary strategies such as low-carb and very-low calory diets regarding their potential to improve metabolism and body weight in (mostly) long-term T2DM patients. This core comparison is dealt with in the DiNA-D study (published elsewhere).

POLYPHEM targets specific dietary approach to preserve the achieved metabolic improvements from DiNA-D phase 1. Nutritional factors will be PUFAs and BCAAs.


Description:

Basic treatment of type 2 diabetes should focus on diet, physical activity and lifestyle. Nevertheless, in early and late stage of T2DM, lifestyle intervention is mostly substituted by pharmacological intervention, although lifestyle modification and dietary treatment would be favourable.

The researchers therefore investigate dietary strategies such as low-carb and very-low calory diets regarding their potential to improve metabolism and body weight in (mostly) long-term T2DM patients. This core comparison is dealt with in the DiNA-D study (published elsewhere).

POLYPHEM targets specific dietary approach to preserve the achieved metabolic improvements from DiNA-D phase 1. Nutritional factors for the maintenance period within DiNA-D (11 months) will be PUFAs and BCAAs, provided by walnuts and custom-made muffins containing walnuts, sunflower oil and isomaltulose.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2020
Est. primary completion date September 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 79 Years
Eligibility Inclusion Criteria:

- male and female subjects

- 18-79 years old

- type 2 diabetes

Exclusion Criteria:

- renal insufficiency

- anaemia

- immunosuppression

- previous symptomatic cancer diagnosis

- acute cardiovascular disease (stroke, coronary syndrome)

- pregnancy and lactation

- severe psychiatric disorders

- corticoid or other immunosuppressive therapy

Study Design


Intervention

Dietary Supplement:
diet with/without supplementation
diet with/without supplementation with PUFAs

Locations

Country Name City State
Germany DIfE (German Institute for Human Nutrition) Berlin

Sponsors (4)

Lead Sponsor Collaborator
German Institute of Human Nutrition California Walnut Commission, German Center for Diabetes Research, Institute for Cereal Processing GmbH/Institut für Getreideverarbeitung (IGV)

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in insulin secretion (glucagon stimulation test) change in insulin secretion (glucagon stimulation test) 49 weeks
Primary change in hepatic fat content (MR-S) change in hepatic fat content (MR-S) 49 weeks
Primary change in insulin secretion in the mixed-meal tolerance test (MMTT) - combined parameter change in insulin secretion in the mixed-meal tolerance test (MMTT) - combined parameter 49 weeks
Primary change in insulin sensitivity in the mixed-meal tolerance test (MMTT) - combined parameter change in insulin sensitivity in the mixed-meal tolerance test (MMTT) - combined parameter 49 weeks
Primary change in blood glucose profile in the mixed-meal tolerance test (MMTT) - combined parameter change in blood glucose profile in the mixed-meal tolerance test (MMTT) - combined parameter 49 weeks
Secondary inflammatory reaction in subcutaneous adipose tissue (SCAT analysis on protein and RNA level - IL-1; IL1beta, IL-6) inflammatory reaction in subcutaneous adipose tissue (SCAT analysis on protein and RNA level - IL-1; IL1beta, IL-6) 49 weeks
Secondary change in parameters of peripheral neuropathy - vibration threshold change in parameters of peripheral neuropathy - vibration threshold 49 weeks
Secondary change in parameters of peripheral neuropathy - thermal sensitivity change in parameters of peripheral neuropathy - thermal sensitivity 49 weeks
Secondary change in parameters of peripheral neuropathy - pain thresholds change in parameters of peripheral neuropathy - pain thresholds 49 weeks
Secondary change in parameters of autonomic neuropathy - measures of cardio-autonomic neuropathy (MSDD) change in parameters of autonomic neuropathy - measures of cardio-autonomic neuropathy (MSDD) 49 weeks
Secondary change in parameters of autonomic neuropathy - measures of cardio-autonomic neuropathy (SANN) change in parameters of autonomic neuropathy - measures of cardio-autonomic neuropathy (SANN) 49 weeks
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