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Clinical Trials/IRCT201312251141N16
IRCT201312251141N16
Completed
Phase 4

Compare the efficacy of two protocols of ovarian stimulation using Gonal-F and Luveris in women with hypogonadotropic hypogonadism undergoing assisted reproductive technique Compare the efficacy of two protocols of ovarian stimulation using Gonal-F and Luveris in women with hypogonadotropic hypogonadism undergoing assisted reproductive technique

Royan Institute0 sites90 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
•Female infertility associated with anovulation.
Sponsor
Royan Institute
Enrollment
90
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Inclusion Criteria:
  • Have a clinical history of hypogonadotropic hypogonadism, and laboratory test result comply with diagnosis of hypogonadotropic hypogonadism; Have discontinued gonadotropins or gonadotropin releasing hormone or estrogen\-progesterone replacement therapy at least one month before the study; Have primary or secondary amenorrhea; Serum LH and FSH \<5\.0 IU/l and oestradiol \<100 pg/ml before initiation of treatment; Have a negative progesterone challenge test; Normal serum concentrations of thyroid stimulating hormone (TSH), prolactin and testosterone within 6 months before the start of study; Have given written informed consent prior to any study related procedure

Exclusion Criteria

  • The other causes of infertility; History of ovarian hyper stimulation syndrome; Abnormal gynecological bleeding of undetermined origin; Previous or current hormone dependent tumor

Outcomes

Primary Outcomes

Not specified

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