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Study on preoperative vaginal biomarkers for complications of mesh exposure during transvaginal pelvic mesh implantation using a prospective clinical cohort

Study on preoperative vaginal biomarkers for complications of mesh exposure during transvaginal pelvic mesh implantation using a prospective clinical cohort

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121964
Enrollment
Unknown
Registered
2026-04-07
Start date
2026-04-07
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Pelvic organ prolapse

Interventions

Observation group with mesh/without mesh:None

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Follow up patients undergoing vaginal mesh implantation surgery;

Exclusion criteria

Exclusion criteria: 1.Sexual activity and vaginal irrigation in the past 5 days; 2.Oral or vaginal antibiotics, antifungal agents, immunosuppressants, hormone drugs, or probiotics used within the past 30 days;

Design outcomes

Primary

MeasureTime frame
Relative abundance of microorganisms;—

Countries

China

Contacts

Public ContactZhibo Zhang

Chinese Academy of Medical Sciences, Peking Union Medical College Hospital

zzbspace@126.com+86 10 69155648

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026