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Application of improved mesh and instrumental in laparoscopic sacrocolpopexy for severe pelvic organ prolapse

Application of improved mesh and instrumental in laparoscopic sacrocolpopexy for severe pelvic organ prolapse

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONN-16009439
Enrollment
Unknown
Registered
2016-10-15
Start date
2016-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

pelvic organ prolapse

Interventions

Group A:Laproscopiccross-shaped sacrocolpopexy
Group B:Laproscopic Y-shaped sacrocolpopexy

Sponsors

Shanghai First Maternity and Infant Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 Years to 80 years; 2. Subject has been diagnosed with uterine prolapse or posthysterectomy vaginal vault prolapse (symptomatic POP-Q stage III or higher) requiring surgical repair; 3. Subject has no uncontrolled systemic disease; 4. Subject is unwilling or unable to give valid informed consent.

Exclusion criteria

Exclusion criteria: 1. Investigator determines subject is not a candidate for surgical repair of her genital prolapse (lack of symptomatic or imaging basis; 2. Subject has active or latent systemic disease (including server liver diseasekidney diseaserespiratory diseasecardiovascular diseaseepilepsy or uncontrolled diabetes; 3. Subject is currently pregnant or intends to become pregnant during the study period; 4. Subject has gynecological or other cancer; 5. Subject is on any medication with could result in compromised immune response, such as immune modulators; 6. Subject is unwilling or unable to give valid informed consent; 7. Subject is unwilling or unable to comply with the requirements of the protocol, complete all quality of Life questionnaires and return for all follow-up visits; 8. Subject with contraindications for laparoscopy.

Design outcomes

Primary

MeasureTime frame
POP-Q;pelvic MRI;

Countries

China

Contacts

Public ContactZhiyuan Dai

Shanghai First Maternity and Infant Hospital

dcydcy2652@sina.com+86 18964535689

Outcome results

None listed

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