- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04068428
Reproductive Health of Couples of Childbearing Age: a Community Based Prospective Cohort Study (ReH-CP)
March 14, 2022 updated by: Zehong Zhou, Guangzhou Women and Children's Medical Center
This community based prospective cohort study was established to investigate the fecundability of couples of childbearing age.
Data are collected regarding age, body mass index, education, menstrual regularity as well as childbearing history.
Results of routine examination of leucorrhea, blood glucose, liver function of the female spouse, and semen analysis of the male spouse are obtained from the National Free Pre-conception Check-up Projects (NFPCP) in China.
Couples recruited will be followed every 6 months for at least 1 year, and their time to pregnancy as well as behavior of seeking medical care would be recorded.
Blood sample and/or information of antral follicle count would be collected from participants who fail to conceive after 12 months of attempts.
Study Overview
Status
Completed
Detailed Description
Infertility is a heavy burden on families, with important implications for individuals and public health.
In the last decades, the trend of delaying marriage and childbearing has further exacerbated the burden of infertility.
From February 2010 to November 2011, a large-scale population-based cross-sectional study was conducted in northern and eastern China.
It was reported that the overall prevalence of infertility was 15.5% among women 'at risk' of pregnancy, and 25.0% among women attempting to become pregnant in China.
The prevalence of infertility was surprisingly high and aroused our great attention.
To further explore the fecundability and associated risk factors in current China, this community based prospective cohort study was established.
Recruitment will be performed at cites of National Free Pre-conception Check-up Projects (NFPCP).
Besides of the information of sociodemographic characteristics and childbearing history of couples, their results of check-ups will also be obtained.
By regular follow-ups, valid data of time to pregnancy will be collected.
A prospective cohort would provide an opportunity to reveal the incidence of infertility, and explore the underlying risk factors of infertility, as well as the demand of assisted reproductive technology.
Study Type
Observational
Enrollment (Actual)
2313
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Guangdong
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Guangzhou, Guangdong, China, 510623
- Guangzhou Women And Children's Medical Center
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Guangzhou, Guangdong, China, 510623
- Tianhe District Maternal and Child Health Hospital
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Hainan
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Haikou, Hainan, China, 570100
- Longhua District Maternal and Child Health Hospital
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Haikou, Hainan, China, 571100
- Qiongshan District Maternal and Child Health Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Couples of childbearing age from the cites of National Free Pre-conception Check-up Projects (NFPCP) in city of Guangzhou in Guangdong Province, or the city of Haikou in Hainan Province, will be recruited.
Description
Inclusion Criteria:
- Couples who finish the national free pre-conception check-up
- Couples who agree to receive follow-ups every half year for at least 1 year
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time to pregnancy
Time Frame: From date of recruitment until the date of last menstrual period when conceived, assessed up to 1 year
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Assessed by calculate the intervals between last menstrual period when conceived and the timing of termination of contraception.
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From date of recruitment until the date of last menstrual period when conceived, assessed up to 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence of infertility
Time Frame: After 1 year of follow-up
|
Infertility was defined according to the World Health Organization manual as failing to achieve pregnancy after at least 12 months of unprotected regular sexual intercourse.
|
After 1 year of follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Zehong Zhou, MD, Guangzhou Women and Children's Medical Center, China
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 26, 2019
Primary Completion (Actual)
December 31, 2020
Study Completion (Actual)
December 31, 2021
Study Registration Dates
First Submitted
August 20, 2019
First Submitted That Met QC Criteria
August 23, 2019
First Posted (Actual)
August 28, 2019
Study Record Updates
Last Update Posted (Actual)
March 16, 2022
Last Update Submitted That Met QC Criteria
March 14, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201925201
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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