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Clinical Trials/IRCT20110908007513N17
IRCT20110908007513N17
Recruiting
Phase 3

Comparative study between three methods of ovulation stimulation, conventional, mild stimulation and combining the stop GnRH agonist with letrozole priming in outcome of poor responders in Assisted Reproductive Technology (ART)

Esfahan University of Medical Sciences0 sites150 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Infertility.
Sponsor
Esfahan University of Medical Sciences
Enrollment
150
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Individuals with poor ovarian response in the ovulation stimulation cycle are characterized by the POSEIDON criterion. Groups 3 and 4 are entered.The third group of patients are under 35 years with abnormal ovarian reserve test AFC (number of antral follicles) less than 5 and antimullerian hormone less than 1\.2 ng / cc. The fourth group of patients are over 35 years with abnormal ovarian reserve test AFC less than 5 And antimullerian hormone less than 1\.2 ng / cc

Exclusion Criteria

  • Patients who are infected with the coronavirus during the cycle, patients who do not respond well to the ovulation stimulation cycle and do not actually have a follicle to empty, patients who received drug incorrectly during the cycle.

Outcomes

Primary Outcomes

Not specified

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