Assessment of Day-night Secretion of Progesterone and LH Across Puberty
NCT ID: NCT02155933
Last Updated: 2023-11-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
75 participants
OBSERVATIONAL
2008-07-10
2025-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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Hyperandrogenemia
Peripubertal girls with hyperandrogenemia
Blood sampling
Blood sampling for later hormone measurements
Controls
Peripubertal girls without hyperandrogenemia
Blood sampling
Blood sampling for later hormone measurements
Interventions
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Blood sampling
Blood sampling for later hormone measurements
Eligibility Criteria
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Inclusion Criteria
* Early and late pubertal girls with hyperandrogenemia
* All subjects will be girls from pre-puberty (Stage 1 breast development and pubic hair growth but at least 7 years old) to 7 years post menarche.
Exclusion Criteria
* Inability to comprehend what will be done during the study or why it will be done
* Hemoglobin \<11.5 g/dL for non-African American subjects; Hemoglobin \< 11.0 g/dL for African American subjects
* Persistently abnormal sodium, potassium, or bicarbonate (i.e., confirmed on repeat)
* Persistently elevated creatinine, hepatic transaminases, or alkaline phosphatase (i.e., confirmed on repeat)
* Total bilirubin \> 1.5 times upper limit of normal (i.e., confirmed on repeat)
* Significant history of cardiac or pulmonary dysfunction (e.g., known or suspected congestive heart failure; asthma requiring intermittent systemic corticosteroids; etc.)
* Untreated hypo- or hyperthyroidism (reflected by persistently abnormal TSH values)
* Total testosterone \> 200 ng/dl
* Basal (follicular) 17-OHP \> 200 ng/ml (in girls without a previous diagnosis of congenital adrenal hyperplasia)
* DHEA-S \> 800 mcg/dl
* Elevation of prolactin \> 2 times upper limit of normal
* Weight less than 25 kg
7 Years
17 Years
FEMALE
Yes
Sponsors
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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
NIH
University of Virginia
OTHER
Responsible Party
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Chris McCartney
Investigator, Center for Research in Reproduction
Principal Investigators
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Christopher R. McCartney, MD
Role: PRINCIPAL_INVESTIGATOR
University of Virginia
Locations
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Center for Research in Reproduction, University of Virginia
Charlottesville, Virginia, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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13502
Identifier Type: -
Identifier Source: org_study_id
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