Hormonal Changes in Early Pregnancy
Public ClinicalTrials.gov record NCT00340028. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Hormonal Changes in Early Pregnancy: Pilot Study to Evaluate Stored Urine Specimens
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
This study will analyze hormones in early pregnancy. Hormonal changes in early pregnancy reflect the quality of implantation in the uterus of the fertilized egg, the function of the corpus luteum (mass of hormone-secreting tissue that forms immediately after ovulation) and placenta, and the health of the embryo. It will determine the following: * Whether early pregnancy hormones vary by characteristics of the mother * Whether early pregnancy hormones differ for pregnancies with male or female babies * Whether early pregnancy hormones can predict the gestational age (age of the baby during pregnancy) and the baby's birth weight * Hormone activity at the time pregnancy symptoms begin * How the contribution of the corpus luteum changes during the pregnancy in different women Stored urine specimens collected from women who participated in the North Carolina Early Pregnancy Study in the 1980s will be used for this study. In addition, to evaluate the quality of the stored samples, new specimens will be collected from women currently enrolled in the University of North Carolina's Right from the Start study. Candidates must be white women not of Latino or Hispanic origin who are between 25 and 35 years of age and who are planning to become pregnant within a few months' time. They must be non-smokers, have regular menstrual cycles, no known fertility problems and no major chronic disease. Urine specimens are analyzed for hormone levels and other changes in early pregnancy that can be measured in urine. Women providing new urine specimens do the following: Pre-Pregnancy The pre-pregnancy part of the study lasts through no more than three consecutive menstrual cycles. Participants who do not become pregnant after three menstrual cycles end the study at that time. * Have a short interview with a study staff member * Complete a daily diary, recording any vaginal bleeding or spotting, health status, and use of medications, and mail the diary to the study office once a week * Use an ovulation testing kit for up to 7 days during their menstrual cycle * Call the study staff within the first 24 hours of becoming pregnant Pregnancy The pregnancy part of the study lasts about 5 weeks. * Continue to complete daily diary records for weekly pickup by staff member * Collect urine samples daily and store them in the freezer for weekly pickup by staff member * Have 1 to 2 tablespoons of blood drawn at home weekly for 4 weeks * Have a brief follow-up telephone interview around week 12 of their pregnancy Urine samples are analyzed for hormones such as human chorionic gonadotropin, estrone-3-glucuronide, and pregnanedrol glucuronide. White blood cells are stored for DNA to study such things as genes controlling hormone metabolism. ...
Study identification
- NCT ID
- NCT00340028
- Recruitment status
- Completed
- Study type
- Observational
- Phase
- Not listed
- Enrollment
- 40 participants
Conditions and interventions
Conditions
Interventions
Not listed
Eligibility (public fields only)
- Age range
- 25 Years to 35 Years
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jan 17, 2005
- Primary completion
- Feb 23, 2006
- Completion
- Apr 21, 2014
- Last update posted
- Dec 31, 2024
2005 – 2014
United States locations
- U.S. sites
- 2
- U.S. states
- 1
- U.S. cities
- 2
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of North Carolina | Chapel Hill | North Carolina | — | — |
| NIEHS, Research Triangle Park | Research Triangle Park | North Carolina | 27709 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00340028, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Dec 31, 2024 · Synced Sep 11, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00340028 live on ClinicalTrials.gov.