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Clinical Trial Summary

Prospective controlled study to assess the reproductive outcomes of OD recipients in which the donors were subjected to the DYG protocol (20mg/day) compared with those subjected to the short protocol with cetrorelix (0.25 mg/day) from Day 7 or since a leading follicle reached 14 mm. The OD cycles were triggered with triptoreline acetate and the trigger criterion was ≥3 follicles of diameter >18mm.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05577806
Study type Observational
Source Clinica de la Mujer Medicina Reproductiva, Chile
Contact
Status Completed
Phase
Start date January 1, 2017
Completion date December 31, 2021

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