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Effect of Chorioamnionitis on Platelet Activation and Placental Vessel Among Preterm Infants by Wnt-Flt1 Signal Pathway

G

Guangdong Women and Children Hospital

Status

Completed

Conditions

Chorioamnionitis
Thrombocytopenia
Preterm Infant
Placenta Diseases

Treatments

Other: chorioamnionitis

Study type

Observational

Funder types

Other

Identifiers

NCT03636698
Guangdong W&C Hospital

Details and patient eligibility

About

Objective:The purpose of this study was to explore the effect and mechanism of maternal chorioamnionitis on placental microvasculature and platelet activation among preterm infants by activating Wnt-Flt1 signal pathway .

Methods:With clinical randomized controlled trial (RCT), the cases were matched with 1:1 according to gestational age and divided into 2 groups according to the placental pathology result: chorioamnionitis group and control group. (1) To observe the platelet parameter, birth weight, thrombrocytopenia and hemorrhage complication, such as intracranial hemorrhage, retinal hemorrhage, pulmonary hemorrhage and gastrointestinal hemorrhage. (2) To observe the miscrovascular density (MVD) in placenta, platelet activating factor (CD62p,CD63) and thrombopotetin (TPO) in preterrn infants.The placental MVD was assessed by immunohistochemical method. The platelet activating factors were detected by flow cytometry. TPO was detected by ELISA. (3) To observe Wnt5a, Flt1 and VEGF in placenta and fetal circulation.The measurement data were analyzed by pair t test and conditional logistic regression. Pearson correlation analysis was used for relationship.

Full description

The exclusive criteria included :(1) born to mother with no any other maternal complications; (2) no congenital abnormalities and neonatal asphyxia; (3) died or discharged within 72 hours.

Enrollment

64 patients

Sex

All

Ages

1+ hour old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. gestational age<37weeks
  2. admitted to the NICU at Guangdong Women and Children Hospital, with a date of birth from June 2016 to December 2016
  3. whose mothers were diagnosed chorioamnionitis by placental histopathology

Exclusion criteria

  1. born to mother with no any other maternal complications
  2. no congenital abnormalities and neonatal asphyxia;
  3. died or discharged within 72 hours.

Trial design

64 participants in 2 patient groups

Chorioamnionitis Group
Description:
preterm infants were born to mothers with chorioamnionitis
Treatment:
Other: chorioamnionitis
Control Group
Description:
preterm infants were born to mothers without chorioamnionitis
Treatment:
Other: chorioamnionitis

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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