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Post Marketing Surveillance of MENOPUR

Post Marketing Surveillance of MENOPUR

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01202123
Enrollment
2501
Registered
2010-09-15
Start date
2008-12-31
Completion date
2014-02-28
Last updated
2014-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

Brief summary

The purpose of this study is to evaluate the safety and efficacy of highly purified (HP) menotrophine to Korean women.

Interventions

None listed

Sponsors

Ferring Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Anovulation in women (WHO group II) * Controlled ovarian hyperstimulation cases for ART

Exclusion criteria

* Hypersensitivity to MENOPUR * Pregnancy, lactation or contraindication to pregnancy * Ovarian cysts not related to polycystic ovarian syndrome * Abnormal uterine bleeding * Tumors in uterus, ovaries and breasts * Ovarian hyperstimulation syndrome * Thromboembolism or history of it * Infertile due to other reason than anovulation * High FSH level indication primary ovarian failure

Design outcomes

Primary

MeasureTime frameDescription
Number of follicles per cycleUp to 6 weeksAn ART cycle: From ovulation (number and size) to when chemical pregnancy test results are recorded

Secondary

MeasureTime frameDescription
Number of adverse eventsUp to 6 weeksAn ART cycle: From ovulation (number and size) to when chemical pregnancy test results are recorded

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026