Nutraceutical on Hyperglycemia

Status Completed

Clinical Trial Summary

Clinical Trial Description

The aim will be to evaluate if Glicoset® 1000, a nutraceutical containing Ilex Paraguariensis, White Mulberry and Chromium Picolinate, can be effective in improving glycemic status in subject with dysglycemia.

The investigators will enroll patients with impaired fasting plasma glucose (IFG) or impaired glucose tolerance (IGT), not taking hypoglycemic agents (both pharmaceuticals or nutraceutical agents). Patients will be randomized to take placebo or Glicoset® 1000 for 3 months, in a randomized, double-blind, placebo-controlled design. Glicoset® 1000 and placebo will be self-administered once a day, 1 tablet during the breakfast. ;

Study Design

Related Conditions & MeSH terms

Dysglycemia

Clinical Trial Details

NCT number	NCT04107922
Study type	Interventional
Source	University of Pavia
Contact
Status	Completed
Phase	Phase 3
Start date	October 1, 2018
Completion date	August 31, 2019

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