Growth Hormone Pretreatment in Poseidon Type IV Undergoing ICSI Using Minimal Induction Protocol:… (NCT05089344) | Clinical Trial Compass
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Growth Hormone Pretreatment in Poseidon Type IV Undergoing ICSI Using Minimal Induction Protocol: A Randomized Controlled Trial
Egypt132 participantsStarted 2021-10-09
Plain-language summary
This study is done aiming to Assess Efficiency of Growth hormone as an adjuvant in pretreatment of Poseidon type IV group " poor responders "undergoing ICSI using minimal induction protocol
Who can participate
Age range35 Years – 42 Years
SexFEMALE
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Inclusion Criteria:
* -Age group between 35 to 42 years old
* AFC \<5
* AMH \<1.2 ng/ml
* first IVF trial
Exclusion Criteria:
* \- Serious and unstable disease, such as cerebrovascular, liver, and kidney disease "will be unfit for pregnancy".
* History of malignant or border line tumors "will be unfit for pregnancy".
* Endocrine or metabolic disorder "affecting quality of oocyte so affecting results".
* Either one of the couple with chromosomal abnormalities "affecting quality of oocyte so affecting results".
* Male partner with severe oligoasthenozoospermia or with teratozoospermia"affecting quality of embryo to be transfered so affecting results".
* Any contraindications to growth hormone, pregnancy (to be ruled out and documented before GH treatment).
* female patients with causes of infertility other than poor ovarian reserve
* females suffering from congenital or acquired uterine anomalies "will affect results of implantation and pregnancy rates "
* females with focal uterine lesions anomalies "will affect results of implantation and pregnancy rates "
* BMI \>30 kg/m2 "affecting quality of oocyte so affecting results".