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Clinical Trial Summary

The accurate identification and efficient management of poor responders remains one of the most enigmatic challenges in assisted reproductive technology (ART). The investigators study will compare the letrozole/antagonist protocol to the hMG/antagonist protocol in women who poor responders.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02158689
Study type Interventional
Source Istanbul University
Contact
Status Completed
Phase N/A
Start date June 2014
Completion date August 2015

See also
  Status Clinical Trial Phase
Completed NCT03438812 - Dehydroepiandrosterone Maintain Mitochondrial Quality of Cumulus Cells in Poor Ovarian Responders N/A
Not yet recruiting NCT05900661 - The Effect of Myo-inositol, Somatropin, and DHEA on Poor Ovarian Responders Phase 2/Phase 3
Recruiting NCT04487925 - Controlled Ovarian Stimulation Versus Modified Natural Cycles in Poor Responders Phase 4
Recruiting NCT02201914 - Clomiphene Citrate Plus Gonadotropins and GnRH Antagonist Versus Flexible GnRH Antagonist Protocol Versus Microdose GnRH Agonist Protocol in Poor Responders Undergoing IVF Phase 4