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NCT06673914

EFFECTS OF OLEUROPEIN ON BLOOD PARAMETERS AND INFLAMMATORY MARKERS IN ADULTS WITH METABOLIC SYNDROME

Active, enrolled NA Last updated 5 November 2024
What this trial tests

NA trial testing Control Group: Diet Group in Metabolic Syndrome in 34 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 November 2024
Primary endpoint
30 December 2024
15 January 2025

Quick facts

Lead sponsorAtlas University
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment34
Start date1 November 2024
Primary completion30 December 2024
Estimated completion15 January 2025
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Atlas University

Who can join

Adults 18 to 49, any sex, with Metabolic Syndrome or Insulin Resistance. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to determine the effect of 6 weeks supplementation of oleuropein on individuals diagnosed with metabolic syndrome. The baseline and end biochemical parameters and anthropometric measurements will be compared with control subjects.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Metabolic Syndrome

Currently open trials in the same condition.

Other Atlas University trials

Trials by the same sponsor.

Verify against primary sources

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/NCT06673914.

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