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The prospect cohort study of MRKH patients managed by a multidisciplinary approach with vaginal dilators

The prospect cohort study of MRKH patients managed by a multidisciplinary approach with vaginal dilators

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066493
Enrollment
Unknown
Registered
2022-12-07
Start date
2022-12-07
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

MRKH syndrome

Interventions

Dilation group:Vaginal dilation

Sponsors

Chinese Academy of Medical Sciences & Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Patients may choose to enter the cohort when they meet all of the following criteria: 1) Normal female karyotype (46, XX); 2) Pelvic ultrasound or MRI diagnoses all or part of the primordial uterus and vagina; 3) After informing the patient of the dilation method and surgical vaginoplasty information, voluntarily choose the dilation method; 4) Age >= 18 years old; 5) Agree to participate in this research.

Exclusion criteria

Exclusion criteria: When a patient has any of the following conditions, she cannot be selected for clinical research: 1) Abnormal karyotype, such as 45,X0 or male karyotype (46,XY; 47,XXY; 47,XYY, etc.) 2) Those who require surgery or surgical vaginoplasty for vaginal narrowing; 3) Refusal to participate in this study.

Design outcomes

Primary

MeasureTime frame
The length of vagina;FSFI;

Secondary

MeasureTime frame
SF-12;PHQ-9, GAD-7;

Countries

China

Contacts

Public ContactLan Zhu

Chinese Academy of Medical Sciences & Peking Union Medical College

zhu_julie@vip.sina.com+86 13911714696

Outcome results

None listed

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