Research and development of innovative method to diagnose pelvic floor dysfunction

Research and development of innovative method to diagnose pelvic floor dysfunction - Research and development of innovative method to diagnose pelvic floor dysfunction

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000039858

Enrollment

300

Registered

2020-03-18

Start date

2020-04-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Pelvic floor dysfunction

Interventions

The vaginal cavity is ultrasonically constructed to measure vaginal wall compliance, by using intravaginal balloon dilation.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1) Patients who visited a gynecological outpatient clinic. 2) Patients whose performance Status is 0-1 can be examined at the obstetrics and gynecology examination table. 3) The consent has been obtained from the person in writing.

Exclusion criteria

Exclusion criteria: 1) Patients whose vaginal cavity is too small to allow internal examination and transvaginal ultrasonography. 2) Patients who cannot undergo internal examination and transvaginal ultrasonography due to pain. 3) Patients with infections in gynecological organs 4) Other patients who are judged by the investigator or participating physician to be ineligible for this study.

Design outcomes

Primary

Measure	Time frame
Intravaginal pressure and volume	—

Secondary

Measure	Time frame
Shape of vagina Tissue compliance measured by elastgraphy	—

Countries

Japan

Contacts

Public ContactMichiko Kodama

Osaka University Graduate School of Medicine Department of Obstetrics and Gynecology

mkodama@gyne.med.osaka-u.ac.jp0668793351

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026