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NCT02912325

Non-Comparative Study to Assess the Efficacy and Safety of the New Food Supplement FaseMETS

Completed NA Last updated 1 October 2019
What this trial tests

NA trial testing Daily administration: 2 tablets FaseMETS a day in Metabolic Syndrome in 34 participants. Completed in 11 June 2018.

Timeline
9 May 2017
Primary endpoint
15 October 2017
11 June 2018

Quick facts

Lead sponsorMDM S.p.A.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment34
Start date9 May 2017
Primary completion15 October 2017
Estimated completion11 June 2018
Sites2 locations across Romania

Drugs / interventions tested

Conditions studied

Sponsor

MDM S.p.A. — full company profile →

Who can join

Adults 45 to 70, any sex, with Metabolic Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective is to evaluate the efficacy of FaseMETS for 6 consecutive months in lowering serum lipids and glucose in subjects with Metabolic Syndrome; The secondary objectives of the trial are: * to evaluate the potential benefit after 3 months of therapy (by an interim analysis) * to evaluate the safety of FaseMETS

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Metabolic Syndrome

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02912325.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing