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
220 participants
OBSERVATIONAL
2015-04-20
2025-12-31
Brief Summary
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Detailed Description
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participants will be asked to be:
1. performed endometrial biopsy
2. taken blood for a few time points (e.g. pre-conception and being pregnant) and to compare different kinds of biochemical markers.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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endometrial biopsy and blood sampling
patient will be performed endometrial biopsy and collected blood samples at particular time points
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Intrauterine adhesions.
* Adenomyosis.
20 Years
40 Years
FEMALE
No
Sponsors
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Chinese University of Hong Kong
OTHER
Responsible Party
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Chung Pui Wah Jacqueline
Associate Professor
Principal Investigators
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Pui Wah Jacqueline Chung, MBBS
Role: PRINCIPAL_INVESTIGATOR
Chinese University of Hong Kong
Locations
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Chinese University of Hong Kong
Hong Kong, , Hong Kong
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2014.637
Identifier Type: -
Identifier Source: org_study_id
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