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A Clinical Evaluation of the Efficacy of the Modified Anterior and Posterior Sacrospinous Ligament Suspension for Apical Prolapse

A Clinical Evaluation of the Efficacy of the Modified Anterior and Posterior Sacrospinous Ligament Suspension for Apical Prolapse

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112713
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Pelvic organ prolapse (POP)

Interventions

Modified sacrospinous ligament suspension group:None
Sacrospinous ligament suspension group:None

Sponsors

Chongqing Health Center for Women and Children
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Women aged >=18 years; 2.Women with midpelvic pelvic organ prolapse (POP) with a pelvic organ prolapse quantification (POP-Q) classification of >=stage II; 3.Women with a follow-up period of at least 6 months; 4.Women who have retained their uterus.

Exclusion criteria

Exclusion criteria: 1.Previous pelvic floor prolapse surgery; 2.Patients with symptomatic uterine myoma, adenomyoma, or endometrial cancer; 3.Patients with chronic pelvic disease; 4.Those with incomplete data.

Design outcomes

Primary

MeasureTime frame
POP-Q score;

Secondary

MeasureTime frame
Postoperative complications;Operative time;Postoperative hospital stay;intraoperative blood loss;

Countries

China

Contacts

Public ContactLiu Lubin

Chongqing Health Center for Women and Children

liulubin1975@126.com+86 23 60354532

Outcome results

None listed

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