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Recruiting NCT02391519

NCT02391519 Effects of High Altitude on AMPK Activation

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Clinical Trial Summary
NCT ID NCT02391519
Status Recruiting
Phase
Sponsor University of Colorado, Denver
Condition Pregnancy
Study Type OBSERVATIONAL
Enrollment 84 participants
Start Date 2016-01
Primary Completion 2026-12-31

Trial Parameters

Condition Pregnancy
Sponsor University of Colorado, Denver
Study Type OBSERVATIONAL
Phase N/A
Enrollment 84
Sex FEMALE
Min Age 18 Years
Max Age 45 Years
Start Date 2016-01
Completion 2026-12-31
Interventions
Collection of myometrial, cord blood, and placental tissue samples

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Brief Summary

Pregnancy elicits adaptive changes in uteroplacental blood flow, which are altered at high altitude and may contribute to the observed 3-fold increase in intrauterine growth restriction (IUGR) and preeclampsia (PreE). The investigators propose to collect myometrial, cord blood, and placental tissue samples from women at high altitude (Summit County) and low altitude (Denver) in Colorado in order to determine if residence at altitude during pregnancy changes the vasoreactivity of myometrial arteries (MA). If altered MA vasoreactivity is found, further studies may be able to link these changes to the increased rates of PreE and IUGR at altitude and contribute to the understanding of these two disorders.

Eligibility Criteria

Inclusion Criteria: * Women scheduled for cesarean delivery at University of Colorado Hospital (Denver, 1600 m) and St. Anthony's Summit Medical Center (Summit County, 3000 m) * Cesarean delivery at a prescheduled time without any labor, typically at 39 weeks gestation Exclusion Criteria: * Women will be excluded if there are co-existing medical diagnoses that are known to affect vascular parameters (i.e., diabetes mellitus, gestational diabetes, any hypertensive disorder of pregnancy, or a current smoker). * Women with multiple gestations and preterm deliveries will also be excluded.

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