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The role of collagen genetic discrepancies in development of pelvic organ prolapse in women

Single nucleotide polymorphisms in type 1 and 3 collagens in women suffering pelvic organ prolapse

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN15002246
Enrollment
250
Registered
2018-01-22
Start date
2017-01-01
Completion date
Unknown
Last updated
2022-10-24

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

Conditions

Pelvic organ prolapse has a mixed etiology – hereditary and acquired. Collagen is playing a major role in pelvic floor supportive structures. The role of single nucleotide polymorphism of the collagen genes remain controversial. This inconsistency has resulted in the current study in which several polymorphisms in collagen in saliva samples of women will be investigated. Urological and Genital Diseases

Interventions

This is cross sectional case-control study evaluating the prevalence of single nucleotide polymorphism (SNP) in collagen type 3 alpha 1 chain (COL3A1), collagen type 1 alpha 1 chain (COL1A1) and coll

Sponsors

Ministry of Health of Russian Federation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Adult women suffering from pelvic organ prolapse and healthy women as controls 2. Aged 18 and older

Exclusion criteria

Exclusion criteria: Hereditary diseases with a known increased risk of POP, such as Marfan or Ehlers-Danlos syndrome and previous surgeries for POP for the control group

Design outcomes

Primary

MeasureTime frame
Single nucleotide polymorphisms in COL3A1 is investigated using Sanger gene sequencing method.

Secondary

MeasureTime frame
1. Single nucleotide polymorphisms in COL1A1 gene is measured using Sanger gene sequencing method 2. Single nucleotide polymorphisms in COL 18A gene is measured using Sanger gene sequencing method

Countries

Russian Federation

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026