Long Term Health Cohort of Premature Infants

Shanghai Jiao Tong University logo

Shanghai Jiao Tong University

Status

Enrolling

Conditions

Preterm

Treatments

Diagnostic Test: Griffiths development scales

Study type

Observational

Funder types

Other

Identifiers

NCT05017389
LY-SCMC2020-01

Details and patient eligibility

About

Establish a clinical diagnosis and treatment and long-term follow-up database of preterm infants, and analyze the effects of prenatal factors (including genetic characteristics, maternal diseases, etc.), postnatal diagnosis and treatment measures and family maintenance environment after discharge on preterm infant mortality and major diseases in the near and long term.

Full description

As an increasing large group, the long-term quality of life and health status of preterm infants have become a very important public health problem in China. This cohort study is a single center clinical cohort study. By collecting the clinical diagnosis, treatment and follow-up data of preterm infants admitted to the neonatal department of our hospital for 3 consecutive years (about 1200 cases), and following them for 18 years, a relatively complete resource database for the long-term health and development of preterm infants is established. The effects of perinatal factors, diagnosis and treatment methods and family rearing environment on the survival rate, neurointelligence development, chronic metabolic diseases and respiratory diseases of preterm infants were analyzed. It provides a basis for further improving the diagnosis and treatment plan, exploring potential therapeutic targets and establishing prediction models.

Enrollment

1,200 estimated patients

Sex

All

Ages

15 days to 4 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Live born newborns with gestational age ≤ 36 + 6 weeks
  • Transfer to the neonatal ward of Shanghai Children's medical center within 24 hours after birth
  • Those who have lived in Shanghai for more than 1 year and plan to live in Shanghai for a long time. Parents voluntarily participated in the study and signed informed consent

Exclusion criteria

  • Premature infants: termination of treatment due to family factors (non-disease reasons) and hospitalization time ≤ 2 weeks
  • Major congenital malformations
  • Parents refuse to participate in the study

Trial contacts and locations

0

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Central trial contact

Shumei Dong, master

Data sourced from clinicaltrials.gov

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