A Multicenter Cohort Study of HPV Viral Load in Predicting the Prognosis of Women With LSIL in Cervix

Status: Recruiting
Location: See all (8) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

Human papillomavirus (HPV) infection has become one of the most important health problems faced by women all over the world. A large number of studies have shown that women's cervical, vaginal and perianal precancerous lesions, related cancers, condyloma acuminatum and other sexually transmitted diseases (STD) are closely related to HPV infection. Among them, the persistent infection of high-risk human papillomavirus (HR-HPV) is closely related to the occurrence of invasive cervical cancer. Previous studies have shown that there are significant differences in the effects of multiple HPV infection and persistent infection of different types (such as type-16, -18, -39 and -52) on different levels of cervical lesions, and there is a certain correlation between HPV load in the process of persistent infection and the degree of cervical lesions. In addition, other studies have shown that HPV-16 viral load has certain clinical significance in predicting Cin2 / CIN3 high-grade cervical lesions, and HPV viral load level is significantly different in cervical low-grade squamous intraepithelial lesion (LSIL) and cervical high-grade squamous intraepithelial lesion (HSIL). The above biological changes such as HPV infection type, quantity and proportion can promote the occurrence and development of cervical precancerous lesions and related cancers to varying degrees. It can be seen that the study of the relationship between HPV viral load and cervical lesions is of great significance for clinical disease development prediction and cervical cancer screening.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 20
Healthy Volunteers: t
View:

• Women aged 20 and over.

• The result of cervical histopathology in the last 3 months was low-grade squamous intraepithelial lesion (LSIL).

• Non pregnant people with sexual history.

• Asexual life, no vaginal medication or flushing before 72 hours of sampling.

Locations
Other Locations
China
Shunde Women's and Children's Hospital of Guangdong Medical University
RECRUITING
Foshan
Fujian Maternity and Child Health Hospital
RECRUITING
Fuzhou
Mindong Hospital of Ningde City
RECRUITING
Ningde
Quanzhou First Hospital Afflicated to Fujian Medical University
RECRUITING
Quanzhou
Maternal and Child Health Hospital of Shenzhen Province
RECRUITING
Shenzhen
Maternal and Child Health Hospital of Hubei Province
RECRUITING
Wuhan
Xiamen Maternity and Child Health Hospital Affiliated to Xiamen University
RECRUITING
Xiamen
Zhangzhou affiliated Hospital of Fujian Medical University
RECRUITING
Zhangzhou
Contact Information
Primary
Binhua Dong
dbh18-jy@126.com
+8613599071900
Time Frame
Start Date: 2021-09-01
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 1000
Treatments
Women with low-grade squamous intraepithelial lesion (LSIL) in cervix
In the enrollment, women whose cervical histopathological results have been diagnosed as low-grade squamous intraepithelial lesion (LSIL) for the last 3 months with abnormal results will be included in this study. All participants will be followed up three times, at 6 months,12 months and 24 months.
Sponsors
Leads: Fujian Maternity and Child Health Hospital

This content was sourced from clinicaltrials.gov