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NCT06085001: Lumella

Use of Lumella-glycosylated Fibronectin for Diagnosis of Preeclampsia

Status unknown Last updated 16 October 2023
What this trial tests

trial testing Lumella finger prick blood test in Preeclampsia in 50 participants. Status unknown.

Timeline
10 November 2023
Primary endpoint
30 May 2024
30 August 2024

Quick facts

Lead sponsorCroydon University Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment50
Start date10 November 2023
Primary completion30 May 2024
Estimated completion30 August 2024
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Croydon University Hospital

Who can join

Eligibility, female only, with Preeclampsia or Pregnancy Related. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

women with symptoms of preeclampsia from antenatal clinic or triage will be offered Lumella test along with traditional blood tests. If Lumella test is positive which will be compared with the traditional blood test results. Once 50 positive cases have been analysed the study results will be submitted to NICE.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Preeclampsia

Currently open trials in the same condition.

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Data sources for this page

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/NCT06085001.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing