- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02323347
Cut-Off Progesterone Values Deleterious for In Vitro Fertilization and Fresh Embryo Transfer
December 22, 2014 updated by: Dr. Francisca Martínez, Institut Universitari Dexeus
At which deleterious cut off value of progesterone on day of HCG (P-hCG) in our IVF program should fresh embryo transfer (ET) be cancelled?
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
There is still an ongoing debate on the effect of subtle increased P-hCG concentration on pregnancy outcome after fresh ET.
No consensus on the cut-off value to define increased P-hCG seems to exist.
It is accepted that high P advances endometrium, leading to asynchrony between the implanting embryo and the endometrium, and resulting in implantation failure.
A freeze all embryos policy and postponement of ET in subsequent frozen-thawed cycle has been proposed.
Study Type
Observational
Enrollment (Actual)
1901
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 49 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Women undergoing IVF-ICSI ad fresh embryo transfer
Description
Inclusion Criteria:
- Fresh embryo transfer
- Progesterone value on day HCG (Human choriogonadotrophin hormone)
Exclusion Criteria:
- Clinical indication for delaying embryo transfer
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 |
Time Frame |
|---|---|
|
Clinical Pregnancy
Time Frame: 6 weeks after embryo transfer procedure
|
6 weeks after embryo transfer procedure
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
January 1, 2009
Primary Completion (Actual)
March 1, 2014
Study Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
December 11, 2014
First Submitted That Met QC Criteria
December 22, 2014
First Posted (Estimate)
December 23, 2014
Study Record Updates
Last Update Posted (Estimate)
December 23, 2014
Last Update Submitted That Met QC Criteria
December 22, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PROGEDEX2014
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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