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Evaluating Pyrroloquinoline Quinone (PQQ) for Improving Obese Pregnancy Outcomes (EPyQ)

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Contents

clinicaltrials.gov/study/NCT06245083
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT062450830
Trial Recruitment Size
300
Trial Sponsor
University of Oklahoma
University of Oklahoma
0
Clinical Trial Start Date
February 22, 2024
0
Primary Completion Date
December 31, 2025
0
Study Completion Date
December 31, 2025
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Prevention0
Intervention Type
Drug0
Interventional Trial Phase
Early Phase 10
Participating Facility
University of Oklahoma Health Sciences Center
University of Oklahoma Health Sciences Center
0
Official Name
Evaluating Pyrroloquinoline Quinone (PQQ) for Improving Obese Pregnancy Outcomes (EPyQ)0
Last Updated
February 7, 2024
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Double0
Masked Party
Investigator0
Participant0

Other attributes

Intervention Treatment
Placebo with soybean oil0
Pyrroloquinoline quinone (PQQ)0
Study summary

Maternal obesity (MO) affects 1 in 5 women and is strongly linked to increased birth weight, childhood/adolescent obesity, life-long metabolic and inflammatory disorders, and childhood neuropsychiatric disorders. There remains a critical unmet need for developing a safe and effective non-pharmacological approach for attenuating metabolic inflammation and ameliorating the adverse effects of MO on offspring health that originate in utero and extend into the lactational period. Pyrroloquinoline quinone (PQQ) is a diet-derived natural food supplement with anti-inflammatory properties that, in humans and mice, improves metabolism and exerts potent immunoregulatory effects at nM-µM doses vs. mM doses for polyphenols. Researchers' central hypothesis is that PQQ administration during MO pregnancy 1) improves maternal metabolic and inflammatory indices, 2) improves utero-placental blood flow and ameliorates placental maladaptation (oxidative stress, hypoxia, inflammation and fatty acid transporter expression) and 3) reduces neonatal adiposity.

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