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Prevalence of FXI gene mutations in women with menorrhagia.

Prevalence of FXI gene mutations in women with menorrhagia. - FXI gene mutations in women with menorrhagia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35784
Enrollment
90
Registered
2011-10-26
Start date
2011-12-02
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

FXI gen mutations

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For patients • Patients with regular heavy menstrual bleeding (=menorrhagia). • Age over 18 years. • Written informed consent.;For healthy volunteers • women with normal menstrual blood loss. • Age over 18 years. • Written informed consent.

Exclusion criteria

Exclusion criteria: For patients: • Patients with postmenopausal, irregular, postcoital and intermenstrual bleeding. • Patients with an intra-uterine device or hormonal treatment. • Patients with anticoagulant, antithrombotic therapy or use of non-steroidal anti-inflammatory drugs (NSAIDs). ;Exclusion criteria for healthy volunteers : • women with postmenopausal, irregular, postcoital and intermenstrual bleeding. • women with an intra-uterine device or hormonal treatment. • women with anticoagulant, antithrombotic therapy or use of non-steroidal anti-inflammatory drugs (NSAIDs).

Design outcomes

Primary

MeasureTime frame
The prevalence and frequency of FXI gene mutations in patients with menorrhagia and healthy volunteers.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)