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Inflammatory Biomarkers for the Diagnosis of oPRES

D

Dunjin Chen

Status

Completed

Conditions

Neutrophil-lymphocyte Ratio
Posterior Reversible Encephalopathy Syndrome
Inflammatory Biomarkers

Treatments

Other: Whether the PE or E patient combined with PRES

Study type

Observational

Funder types

Other

Identifiers

NCT05433870
2019B08

Details and patient eligibility

About

The purpose of this study is to explore the inflammatory biomarkers for the diagnosis of obstetric posterior reversible encephalopathy syndrome.

Full description

The investigators retrospectively collected data (General information, clinical data, biochemical indicators, imaging features, and pregnancy outcome) from pregnant woman diagnosed with PRES to explore the inflammatory biomarkers for the diagnosis of oPRES during 2012 to 2021.Then, the investigators grouped all the patients into PRES group (PE or E with PRES) and NOT-PRES group (PE or E without PRES) according to the diagnostic criteria of PRES. Then, the investigators analysed the inflammatory biomarkers, such as neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), monocyte-lymphocyte ratio (MLR), and so on of two groups, and compared the difference of tow groups.

Enrollment

621 patients

Sex

Female

Ages

16 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Pregnant women were diagnosed of PE or E.
  2. All patients were examined the cranial imaging (MRI or CT), and imaging findings meeting the diagnostic criteria of PRES or normal.
  3. all patients provided written informed consent.

Exclusion criteria

  1. patients combined with other neurological disorders
  2. patients combined with mental illness

Trial design

621 participants in 2 patient groups

PRES group
Description:
patients in PE or E with PRES
Treatment:
Other: Whether the PE or E patient combined with PRES
NON-PRES group
Description:
patients in PE or E without PRES

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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