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NCT06673914Active, not recruiting

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

Source: ClinicalTrials.gov · Last updated 5 Nov 2024

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
34 (actual)
First submitted
23 Jul 2024
Start date
1 Nov 2024
Primary completion date
30 Dec 2024
Lead sponsor
Atlas University
Diseases
Obesity
NCT number
NCT06673914

What you commit to

  • Study type: Interventional
  • Participants enrolled: 34
  • From 1 Nov 2024 to the primary completion date, 30 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Starting to use any medication or nutritional supplement during the study

Other illness

  • Occurrence of the problem and/or infection
  • Failure to comply with the regulated medical nutrition treatment
  • Failure to participate in routine meetings and failure to complete necessary measurements

Other

  • The patient included in the study leaves the study
  • Any health issues that may affect the results of the research during the research.
  • Becoming pregnant during the research
  • Being in the experimental group and not consuming extract regularly
  • Leaving study voluntarily

Who the study is looking for

  • Individuals who volunteer to participate in the study by signing the voluntary consent form
  • Diagnosed with Metabolic Syndrome
  • Individuals who did not have any infection at the time the study started
  • Not consuming any medication
  • Not pregnant or lactating
  • Women aged 18-49 who have not entered menopause and men in the same age group
  • Willing to consume the given extract
  • Not allergic or intolerant to olive leaves
  • No history of drug use
  • People with a BMI below 40 kg/m2

Age in the registry: 18 years to 49 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Atlas University
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.