Application of pessary in patients with pelvic organ prolapse and analysis of related factors

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500096256

Enrollment

Unknown

Registered

2025-01-21

Start date

2025-01-31

Completion date

Unknown

Last updated

2025-01-27

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

Conditions

pelvic organ prolapse

Interventions

Test group:Appropriate size pessary was selected for wearing

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: (1) Voluntary test and signed informed consent; (2) POP-Q index >=II degree; (3) All successful pessary wearers; (4) accompanied by varying degrees of urinary incontinence and vaginal symptoms; (5) Pelvic and cervical cytology were normal.

Exclusion criteria

Exclusion criteria: (1) Combined with acute inflammation of reproductive tract; (2) Vaginal cervical lesions; (3) Combined with malignant tumor; (4) Allergic to pessary materials.

Design outcomes

Primary

Measure	Time frame
Pelvic Organ Prolapse Quantification;Pelvic floor distress inventory;Pelvic Floor Impact Questionnaire;Vaginal microbiological test;	—

Secondary

Measure	Time frame
Pelvic floor muscle strength;Visual analog scale;	—

Countries

China

Contacts

Public ContactLedan Wang

The Second Affiliated Hospital of Wenzhou Medical University

ledanwang331@163.com+86 138 5885 0907

Outcome results

None listed

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