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Clinical Application Study of the Self-Adjusting Net Support Device for Pelvic Organ Prolapse with I-Level Support

Clinical Application Study of the Self-Adjusting Net Support Device for Pelvic Organ Prolapse with I-Level Support

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117524
Enrollment
Unknown
Registered
2026-01-26
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

pelvic organ prolapse

Interventions

Prefabricated Mesh Group:NA
Customized Mesh with Regulator Group:NA

Sponsors

Meishan City Peoples Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Patients with severe third-degree or higher prolapse that significantly impairs quality of life; 2. Patients who show poor response to non-surgical treatment or cannot tolerate it; 3. Patients who experience recurrence after non-mesh surgical treatment; 4. Patients with isolated anterior pelvic organ prolapse.

Exclusion criteria

Exclusion criteria: 1. Sexually active and premenopausal women face increased risks of sexual discomfort and mesh exposure; 2. Patients with a history of pelvic radiation therapy, where local anatomical layers are compromised due to radiation, are at higher risk of injury and mesh exposure; 3. Patients with chronic pelvic pain; 4. Individuals with local conditions preventing hip abduction, necessitating the lithotomy position.

Design outcomes

Primary

MeasureTime frame
POP-Q rating;Quality of Life Rating;Intraoperative and short-term postoperative conditions;Imaging Evaluation;

Secondary

MeasureTime frame
Complications and Adverse Events;

Countries

China

Contacts

Public ContactYang Qin

Meishan City Peoples Hospital

41433978@qq.com+86 28 38025132

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026