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NCT04990141: PREMOM

Molecular Screening Method for Preeclampsia (PREMOM)

Completed Last updated 25 March 2025
What this trial tests

trial testing Peripheral blood collection in cases group in Preeclampsia in 9,586 participants. Completed in 27 March 2024.

Timeline
23 September 2021
Primary endpoint
27 March 2024
27 March 2024

Quick facts

Lead sponsoriPremom
StatusCompleted
Study typeOBSERVATIONAL
Enrollment9,586
Start date23 September 2021
Primary completion27 March 2024
Estimated completion27 March 2024
Sites15 locations across Spain

Drugs / interventions tested

Conditions studied

Sponsor

iPremom

Who can join

18 and older, female only, with Preeclampsia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Preeclampsia (PE) is a major obstetric complication with short- and long-term consequences for the mother and the fetus. Early screening tools to reduce its mortality and morbidity, as well as to prevent the life-threatening consequences are needed. Thus, the detection of women at risk of suffering PE is key to apply preventive and treatment strategies. Recently, the maternal contribution to PE based on defective decidualization has been evidenced and new technical approaches developed to detect circulating biomolecules in blood such as RNA fragments. The main objective of this study is to evaluate the diagnostic precision of the molecular profile from the maternal blood analysed for the early screening of early onset preeclampsia (EOPE).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Maternal plasma cell-free RNA as a predictor of early and late-onset preeclampsia throughout pregnancy.
    Castillo-Marco N, Cordero T, Igual M, Muñoz-Blat I, et al · · 2025 · PMID 41115885 · DOI 10.1038/s41467-025-64215-2

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Other recruiting trials for Preeclampsia

Currently open trials in the same condition.

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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/NCT04990141.

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