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CompletedNCT01202123Updated Feb 21, 2014

Post Marketing Surveillance of MENOPUR

An observational study in Infertility, sponsored by Ferring Pharmaceuticals. Completed at 19 sites in Korea, Republic of. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-02-21.

Sponsored by Ferring Pharmaceuticals · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
2,501
Ages
18 Years and older
Sex
Female
01

Study summary

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

02

Conditions studied

  • Infertility

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03

In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's enrollment of 2,501 is above the median of 200 across 714 observational studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

Ferring Pharmaceuticals is the lead sponsor of 244 studies on the registry; 4 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 13 (93%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Infertile women

Inclusion criteria

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

Exclusion criteria

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
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
2,501 participants (actual)
06

What researchers measure

Primary outcomes

  1. Number of follicles per cycle

    An ART cycle: From ovulation (number and size) to when chemical pregnancy test results are recorded

    Time frame: Up to 6 weeks

Secondary outcomes

  1. Number of adverse events

    An ART cycle: From ovulation (number and size) to when chemical pregnancy test results are recorded

    Time frame: Up to 6 weeks

07

Study locations

19 sites
  • Miz Women's Hospital
    Daejeon, Daejeon Metropolitan City, Korea, Republic of
  • Seoul´s Women´s Hospital
    Bucheon, Gyeonggi Province, Korea, Republic of
  • Ilsan Maria Hospital
    Ilsan, Gyeonggi Province, Korea, Republic of
  • Premedi Women's Clinic
    Kwangju, Kwangju Metropolitan City, Korea, Republic of
  • Gumi CHA University Medical Center
    Gumi, Kyoungbuk Province, Korea, Republic of
  • Mama Papa & Baby Hospital
    Ulsan, Kyoungnam Province, Korea, Republic of
  • Busan Maria hospital
    Busan, Korea, Republic of
  • Daegu Maria
    Daegu, Korea, Republic of
  • Daejeon Maria
    Daejeon, Korea, Republic of
  • Daejeon Seoul Women Hospital
    Daejeon, Korea, Republic of
  • Ellemedi Women Clinic
    Daejeon, Korea, Republic of
  • Incheon Seoul women Hospital
    Incheon, Korea, Republic of
  • Cheil General Hospital & Women's Healthcare Center
    Seoul, Korea, Republic of
  • Gangseo Mizmedi Hospital
    Seoul, Korea, Republic of
  • Hamchoon women clinic
    Seoul, Korea, Republic of
  • Maria Plus Hospital
    Seoul, Korea, Republic of
  • Samsung Medical Center
    Seoul, Korea, Republic of
  • Songnae Maria Hospital
    Seoul, Korea, Republic of
  • Maria Hospital
    Seoul, ´Shinseoul-dong, Dongdaemun-gu, Korea, Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 21, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01202123
Lead sponsor
Ferring Pharmaceuticals
Responsible party
Sponsor
First posted
Sep 15, 2010
Start date
Dec 2008
Primary completion
Nov 2013
Completion
Feb 2014
Last update
Feb 21, 2014

Study contacts

Clinical Development Support
study director · Ferring Pharmaceuticals

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2014. You cannot join it, but the record below documents what was studied.

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