The Clinical and Prognostic Features of PRES

NCT05143710 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 354

Last updated 2022-03-02

No results posted yet for this study

Summary

The purpose of this study is to determine the features of clinical imaging, disease severity and pregnancy outcomes in posterior reversible encephalopathy syndrome with preeclampsia or eclampsia.

Conditions

  • Posterior Reversible Encephalopathy Syndrome
  • Pregnancy Outcomes
  • Preeclampsia
  • Eclampsia

Interventions

DIAGNOSTIC_TEST

PRES in PE or E

patients diagnosed with posterior reversible encephalopathy syndrome with preeclampsia or eclampsia

Sponsors & Collaborators

  • Dunjin Chen

    lead OTHER

Eligibility

Min Age
16 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-10-01
Primary Completion
2022-01-31
Completion
2022-01-31

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05143710 on ClinicalTrials.gov