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NCT05433870
Inflammatory Biomarkers for the Diagnosis of oPRES
trial testing Whether the PE or E patient combined with PRES in Posterior Reversible Encephalopathy Syndrome in 621 participants. Completed in 31 July 2022.
31 July 2022
Quick facts
| Lead sponsor | Dunjin Chen |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 621 |
| Start date | 1 July 2022 |
| Primary completion | 31 July 2022 |
| Estimated completion | 31 July 2022 |
| Sites | 1 location across China |
Drugs / interventions tested
- Whether the PE or E patient combined with PRES
Conditions studied
- Posterior Reversible Encephalopathy Syndrome — all drugs for Posterior Reversible Encephalopathy Syndrome →
- Inflammatory Biomarkers — all drugs for Inflammatory Biomarkers →
- Neutrophil-lymphocyte Ratio — all drugs for Neutrophil-lymphocyte Ratio →
Sponsor
Dunjin Chen — full company profile →
Who can join
Adults 16 to 50, female only, with Posterior Reversible Encephalopathy Syndrome or Inflammatory Biomarkers. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to explore the inflammatory biomarkers for the diagnosis of obstetric posterior reversible encephalopathy syndrome.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT05433870
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Posterior Reversible Encephalopathy Syndrome
Currently open trials in the same condition.
- NCT03470467 — Posterior Reversible Encephalopathy Syndrome in the Critically Ill Patients · recruiting
Other Dunjin Chen trials
Trials by the same sponsor.
- NCT06684080 — The Effectiveness of a Care Bundle to Prevent Postpartum Hemorrhage After Cesarean Delivery · NA · not yet recruiting
- NCT05310513 — The Predictors of ICU Admission of oPRES · completed
- NCT05143710 — The Clinical and Prognostic Features of PRES · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05433870 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Dunjin Chen
- Last refreshed: 3 August 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05433870.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing