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Effects of Hydroxytyrosol Administration in Anthropometric Parameters in Overweight and Obese Women

NCT04317079 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2020-03-20

No results posted yet for this study

Summary

This study aims to investigate the potential effects of the administration of hydroxytyrosol, which is an extra virgin olive oil phenolic compound, in doses 15 milligrams and 5 milligrams daily versus placebo for 6 months in anthropometric parameters such as body weight, body fat and visceral fat, in combination with diet, in overweight and obese women.

Conditions

  • Body Weight
  • Visceral Obesity

Interventions

DIETARY_SUPPLEMENT

Hydroxytyrosol

Administration of hydroxytyrosol in doses 15mg and 5 mg compared to placebo for 6 months

OTHER

Diet

Consultation by a dietitian was offered to all participants

Sponsors & Collaborators

  • National and Kapodistrian University of Athens

    lead OTHER

Principal Investigators

  • Nikolaos Tentolouris, MD,PhD · National Kapodistrian University of Athens

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
66 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-10-30
Primary Completion
2019-05-15
Completion
2019-05-15

Countries

  • Greece

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04317079 on ClinicalTrials.gov