Antagonist Protocol in Poor Responders (NCT02195947) | Clinical Trial Compass
CompletedPhase 4
Antagonist Protocol in Poor Responders
Egypt141 participantsStarted 2014-07
Plain-language summary
The effect of use of the growth hormone with antagonist protocol on the outcome of the IVF/ICSI cycles in poor responders.
Who can participate
Age range20 Years – 45 Years
SexFEMALE
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Inclusion Criteria:
* females fulfilling the criteria of the ESHRE consensus 2011:
* at least two of the following three features must be present:
* dvanced maternal age (≥40 years) or any other risk factor for POR
* previous POR (≤3 oocytes with a conventional stimulation protocol)
* an abnormal ovarian reserve test (i.e. AFC ,5-7 follicles or AMH ,0.5 -1.1 ng/ml).
Exclusion Criteria:
* women who suffer from any other cause of infertility other than poor ovarian reserve
* refusal of the patient to consent for using her data in the study.