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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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16 December 2017 |
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Main ID: |
NCT02189369 |
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Date of registration:
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10/07/2014 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Diagnostic Test for Endometrial Receptivity 24 Hours Before Embryo Transfer
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Scientific title:
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Clinical Validation of a Diagnostic Test Which Measures the Endometrial Prostaglandins Liquid 24 Hours Before Embryo Transfer and That is Capable of Predicting a State of Endometrial Receptivity |
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Date of first enrolment:
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February 2015 |
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Target sample size:
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120 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02189369 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized. Intervention model: Parallel Assignment. Primary purpose: Basic Science. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Spain
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Contacts
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Name:
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Carlos Simon, MD PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Fundación IVI |
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Name:
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Carlos Gómez, MA |
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Address:
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Telephone:
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+34670506469 |
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Email:
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carlos.gomez@igenomix.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Any IVF patient being treated for single or double embryo transfer
- BMI: 20 - 30
- Normal ovarian response (7 - 8 ovocitos) in IVF treatment with AFC = 8, (AFC = Antral
Follicle Count)
- Elective embryo transfer
- Normal uterine cavity
- Age: = 38 years old for patients with own oocytes; = 50 years old for patients with
donated oocytes.
Exclusion Criteria:
- Patients with recurrent miscarriages ( = 2 biochemical miscarriages; = 2 clinical
miscarriage)
- Patients with severe male factor ( = 2*106 espermatozoides/ml).
Age minimum:
18 Years
Age maximum:
50 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Infertility
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Intervention(s)
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Other: Day 5 embryo transfer
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Other: Day 3 embryo transfer
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Primary Outcome(s)
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endometrial receptivity
[Time Frame: 24 hours before embryo transfer]
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Secondary Outcome(s)
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Implantation rate
[Time Frame: 15 days]
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Pregnancy rate
[Time Frame: 15 days]
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Secondary ID(s)
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1311-FIVI-135-CS
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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