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The value of cervical microenvironmental next-generation sequencing macrogenomic analysis in the diagnosis, treatment and progression prediction of cervical lesions

The value of cervical microenvironmental next-generation sequencing macrogenomic analysis in the diagnosis, treatment and progression prediction of cervical lesions

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068479
Enrollment
Unknown
Registered
2023-02-21
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Cervical cancer and cervical intraepithelial neoplasia

Interventions

Case series:not applicable

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, pre-menopausal. 2. those with suspected cervicitis, cervical erosion, cervical polyps, cervical intraepithelial neoplasia, cervical cancer and other cervical diseases or health check-ups 3. Those who need to undergo cervical cytology and HPV screening for routine medical treatment. 4. Those who obtained informed consent.

Exclusion criteria

Exclusion criteria: 1. Insufficient sample collection, confused records or have been contaminated beyond the user. 2. A previous history of neoplasm other than cervical cancer 3. Those who have received immunosuppressive therapy or anti-infective treatment within the last two weeks 4. In the state of pregnancy or within 8 weeks after delivery 5. History of sub/total hysterectomy or treatment of cervical injury prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Cervical cytology;Human papillomavirus infection;Cervical histopathology;Metagenomic sequencing data;

Countries

China

Contacts

Public ContactXu Xiaogang

Huashan Hospital, Fudan University/Institute of Antibiotics

xuxiaogang@fudan.edu.cn+86 138 1750 7007

Outcome results

None listed

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