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Clinical Trial Summary

This is a randomized controlled clinical trial to investigate the effect of dual trigger (hCG and GnRH agonist) on the final oocyte maturation compared to the standard hCG trigger in patients with poor ovarian reserve seeking IVF/ICSI treatment.


Clinical Trial Description

Women with POR (Bologna criteria) manifest a very low follicular response to controlled ovarian stimulation irrespective of the stimulation protocol utilized. Dual triggering of oocyte maturation was shown to improve follicle collection yield and oocyte maturation in women with predicted normal ovarian response. These benefits have been attributed to the GnRHa-induced FSH surge believed to promote oocyte nuclear maturation and cumulus expansion. The aim of the study is to show whether the co-administration of a GnRH agonist and hCG for final oocyte maturation improve oocyte collection and maturation rate ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04224818
Study type Interventional
Source American University of Beirut Medical Center
Contact
Status Completed
Phase Phase 3
Start date July 11, 2018
Completion date August 30, 2019

See also
  Status Clinical Trial Phase
Completed NCT01204840 - Growth Hormone for Poor Responders in in Vitro Fertilization (IVF) Phase 2
Completed NCT04797377 - Autologous Intraovarian Platelet Rich Plasma Treatment in Women With Poor Ovarian Response N/A
Recruiting NCT05602090 - Growth Hormone For Poor Ovarian Reserve Patients in ICSI Trials Phase 2/Phase 3
Not yet recruiting NCT04588844 - Effect of Growth Hormone Injection on the IVF/ICSI Outcome of Patients With Poor Ovarian Reserve. N/A