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Status unknownNCT00619333Updated Jan 12, 2010

Inactive FSH in Galactosemia

An interventional study of follitropin and lutropin in Galactosemia and Premature Ovarian Failure, sponsored by Maastricht University Medical Center. Status unknown at 1 site in Netherlands. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-01-12.

Sponsored by Maastricht University Medical Center · Not applicable and Interventional

The sponsor has not verified this record recently (last verified Jan 2010), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Ages
18 Years and older
Sex
Female
01

Study summary

The aim of the study is to investigate whether inactive FSH plays a role in the development of Premature Ovarian Failure in women with Classic Galactosemia

02

Conditions studied

  • Galactosemia
  • Premature Ovarian Failure
03

In context

Primary Ovarian Insufficiency

172 studies on the registry are indexed under Primary Ovarian Insufficiency; 45 are open to participants now.

This study's planned enrollment of 25 is below the median of 49 across 109 interventional studies indexed under Primary Ovarian Insufficiency.

Browse Primary Ovarian Insufficiency studies →

Lead sponsor

Maastricht University Medical Center is the lead sponsor of 835 studies on the registry; 122 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosis of galactosemia through GALT-activity analysis and/or mutation analysis
  • Premature Ovarian Failure with FSH > 30 U/l

Exclusion criteria

Exclusion Criteria:

  • Gynecological cancers and/or unexplained vaginal bleeding
05

Study design

Phase
Not applicable
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (estimated)

Study arms

  • Other
    1

    Drug: follitropin and lutropin

Interventions

  • Drugfollitropin and lutropin

    follitropin and lutropin

06

What researchers measure

Primary outcomes

  1. Estradiol response

    Time frame: 3 days

07

Study locations

1 site
  • Maastricht University Hospital
    Maastricht, Netherlands
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 12, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00619333
Lead sponsor
Maastricht University Medical Center
Collaborators
The Dutch Galactosemia Society
First posted
Feb 20, 2008
Start date
Mar 2007
Primary completion
Mar 2010 (estimated)
Last update
Jan 12, 2010

Study contacts

Estela Rubio-Gozalbo, MD, PhD
principal investigator · Maastricht University Hospital

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jan 2010. You cannot join it, but the record below documents what was studied.

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