Genetics of pelvic organ prolapse; identification of specific gene defects in patients and their family members.

Genetics of pelvic organ prolapse; identification of specific gene defects in patients and their family members. - Genetics of pelvic organ prolapse

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON33518

Enrollment

Registered

2009-06-16

Start date

2009-06-22

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

Pelvic organ prolapse Urogenital prolapse

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: First and second degree relatives of patients with COL3A1 2209G>A polymorphism

Exclusion criteria

Exclusion criteria: -Genetic diseases with a known increased risk of POP (such as Ehlers Danlos, Marfan and Steinert*s disease) -Problems with regards to the patient*s understanding of the study

Design outcomes

Primary

Measure	Time frame
Presence of the COL3A1 2209G>A polymorphism in family members of patients with the homozygous form of this polymorphism.	—

Secondary

Measure	Time frame
Presence of pelvic organ prolapse and related conditions such as inguinal hernia in family members of patients with the homozygous form of the COL3A1 2209G>A polymorphism.	—

Countries

Netherlands

Outcome results