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Predictive Model for Prognosis of Chronic HBV Infection Mothers (PMFPOEPMWCHI)

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Xi'an Jiaotong University

Status

Unknown

Conditions

Hepatitis B, Chronic

Treatments

Other: Age, BMI,Baseline HBV DNA, Baseline HBeAg level, Baseline HBsAg level, Antiviral treatment, Serum ALT level

Study type

Observational

Funder types

Other

Identifiers

NCT04805034
XJTU1AF-CRF-2020-001

Details and patient eligibility

About

Pregnancy is a complex and coordinated physiological process. Pregnancy and the postpartum period are associated with unique changes in the immune system that may impact the natural history of autoimmune diseases and immune-mediated infections. In the postpartum period. ALT flares have been reported in 20%-60% of untreated women and were more likely to occur in hepatitis B e antigen (HBeAg)-positive patients. It has been postulated that postpartum ALT flares may arise to rapid immune restitution against hepatitis B virus (HBV) antigens in the liver, when may be a timing of antiviral treatment. A large number of previous studies have focused on studies on the interruption of mother-to-child transmission in women with chronic hepatitis B(CHB), but studies on the prognosis of mothers undergoing pregnancy and delivery are very limited. What are the factors that affect the clearance of HBeAg or HBsAg? What kind of antiviral treatment protocol should be adopted for mothers with CHB? It is not only a problem that needs to be solved urgently in clinical practice, but also can provide some clues for understanding the occurrence and development of HBV infection in women of childbearing age.

Overall, this study intends to carry out a multi-center two-way cohort study on E antigen-positive CHB women in 9 hospitals in Shaanxi Province. To observe the dynamic changes of virological parameters in these patients, figure out the factors of the serum HBsAg loss and HBeAg seroconversion, and establish relevant predictive models.

Enrollment

1,600 estimated patients

Sex

Female

Ages

20 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 20-45 years old
  • Serum HBsAg positive> 6 months
  • HBeAg positive at delivery
  • Good compliance

Exclusion criteria

  • Women who give birth to stillbirth due to various reasons
  • Coinfection with HIV,HCV, syphilis or other sexually transmitted diseases
  • Severe kidney, cardiovascular, lung, nervous system or immune system diseases
  • Who are taking immunotherapy drugs or anti-tumor drugs

Trial design

1,600 participants in 2 patient groups

HBeAg positive/HBsAg positive
Treatment:
Other: Age, BMI,Baseline HBV DNA, Baseline HBeAg level, Baseline HBsAg level, Antiviral treatment, Serum ALT level
HBeAg seroconversion /HBsAg loss
Treatment:
Other: Age, BMI,Baseline HBV DNA, Baseline HBeAg level, Baseline HBsAg level, Antiviral treatment, Serum ALT level

Trial contacts and locations

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Central trial contact

Naijuan Yao, phD; Tianyan Chen, phD

Data sourced from clinicaltrials.gov

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