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Cervical Cancer Susceptible Population Classification

Evalutaion of the SNPs Test in Average Cervical Cancer Screening Episode

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06405945
Enrollment
10000
Registered
2024-05-09
Start date
2024-05-01
Completion date
2036-06-30
Last updated
2024-05-09

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

Conditions

Cervical Cancer Susceptible Population Classification

Brief summary

Cervical cancer is the third most common lethal tumor globally, causing around a quarter million deaths annually, despite the availability of HPV vaccines. Recent Genome-wide association studies (GWAS) have identified numerous genetic markers linked to cervical cancer, including rs10175462, rs10007915, rs35721900, and rs61646675, which have been verified as being related to susceptibility to cervical cancer. However, many reports lack clarity, consistency, and validation. In this comprehensive study, we will analyze the genomic risk factors associated with cervical cancer, classify individuals into different risk categories, and explore potential biomarkers and therapeutics.

Interventions

GENETICPCR and sequence

sequence the mutatation SNPs

Sponsors

Anhui Provincial Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Subjects aged \>=18 years at time of consent 2. Intended to undergo screening colposcopy 3. Considered by a physician or healthcare provider as being of average risk for cervical cancer 4. Willing to consent to blood draw cervical disease treatments 5. Willing to sonsent to follow-up for five years as per protocol

Exclusion criteria

1. History of cervical cancer 2. History of any malignancy (patients who have undergone surgical removal of skin squamous cell cancer may be enrolled provided the procedure was completed at least 12 months prior to the date of provision of informed consent for the study) 3. Currently taking any anti-neoplastic or disease-modifying anti-rheumatic drugs. 4. Any major physical trauma (e.g. disruption of tissue, surgery, organ transplant, blood product transfusion) within the 30 days leading up to the provision of informed consent 5. Known medical condition which, in the opinion of the investigator, should preclude enrollment into the study

Design outcomes

Primary

MeasureTime frame
Evalutaiton of the SNPs test in an average cervical cancer patients screening episodetwo years

Secondary

MeasureTime frame
Classified susceptied person into different ladderstwo years

Countries

China

Contacts

Primary ContactYingying Wang, Doctor
yingyingwang@ustc.edu.cn18652270921
Backup ContactTingting Zhao, Master
heyppy@163.com17333296213

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026