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Polyphenols Supplementation on Prostaglandin E2 in Women - Randomized Clinical Trial

Polyphenol Supplementation Inhibits Physiological Increase of Prostaglandin E2 During Reproductive Period - A Randomized Clinical Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02567617
Enrollment
26
Registered
2015-10-05
Start date
2014-05-31
Completion date
2015-03-31
Last updated
2015-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Disorder of the Cardiovascular System

Keywords

Polyphenols, Prostaglandin E2, hormonal contraceptives

Brief summary

The aim of this study was to evaluate the effect of polyphenol supplementation on plasma levels of prostaglandin E2 in women during the reproductive period.

Detailed description

The effect of anti-inflammatory substances on the constriction of the fetal ductus arteriosus is well documented, but the anti-inflammatory property of polyphenols and their effect on the metabolism of prostaglandins are not established. Evidence indicates that foods rich in polyphenols consumed from the third trimester of pregnancy may interfere with anatomical and functional activity of the fetal heart, presumably by the action similar to anti-inflammatory drugs nonsteroidal, causing inhibitory effect on prostaglandin synthesis. Objective: The objective of this study was to evaluate the effect of polyphenol supplementation on plasma levels of prostaglandin E2 in women of childbearing age use of hormonal contraceptives. As secondary endpoints were also evaluated other markers of inflammation and oxidative stress. The selected women were randomized to receive capsules polyphenol at a concentration of 3000 mg / day or placebo capsules to be consumed daily for fifteen days. Was applied dietary recall to assess intake of polyphenols, measured height and weight and carried blood samples for prostaglandin analysis E2 (PGE2), high sensitive C-reactive protein, and urine for analysis of total polyphenols and F2 isoprostane (8 iso-PGF2a). Statistical analysis: The results will be expressed through absolute and relative frequencies and mean ± standard deviation (SD) or median and interquartile range. For analysis, Pearson correlation is used. To compare the means will be used Student's t test. The level of significance is 5%. Considering a 90% power, with absolute error margin of 5% in the present study, 13 patients were needed in each group.

Interventions

DIETARY_SUPPLEMENTPolyphenols

Capsules with five substances (polyphenols) at a concentration of 3000mg per day

DIETARY_SUPPLEMENTPlacebo controlled

Starch capsules

Sponsors

Instituto de Cardiologia do Rio Grande do Sul
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Women aged 25 to 35 * Use of hormonal contraceptives * Agreed to participate and signed the Informed Consent

Exclusion criteria

* Pregnant women * Use of anti-inflammatory drugs * Using supplementation of omega 3 * BMI higher than 30 kg / m² * Previous diagnosis of diabetes mellitus, hypertension, dyslipidemia, malignancy or infection

Design outcomes

Primary

MeasureTime frameDescription
Prostaglandin E2Baseline; 15 daysmarkers analyzed in plasma

Secondary

MeasureTime frameDescription
F2 isoprostaneBaseline; 15 daysmarker analyzed i urine

Other

MeasureTime frameDescription
High sensitive C reactive proteinBaseline; 15 daysmarkers analyzed in plasma

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026