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NCT02527018 · ClinicalTrials.gov registry record

A Comparison of BNP Levels Using the Nexfin Device in Healthy Pregnant and Preeclamptic Women

A clinical trial, sponsored by University of California, Irvine.

Completed
Registry status
66
Enrollment target

NCT02527018: Completed study, sponsored by University of California, Irvine.

NCT02527018 is a clinical trial that has completed, run by University of California, Irvine. The registered enrollment target is 66 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02527018 has completed, sponsored by University of California, Irvine.

COMPLETED
Registry status
66 participants
Enrollment target

Study Summary

Primary Endpoint: Quantify the hemodynamic changes in preeclampsia using the non-invasive Nexfin device. Secondary Endpoint: Determine if measurable hemodynamic changes are statistically correlated with B-type natriuretic peptide (BNP) levels.

Primary Outcome

Composite Changes are defined by volume overload (mL), higher B-type natriuretic peptide levels pg/mL, higher blood pressure or cardiac output (mm / Hg).

Interventions

  • DEVICE Sphygmomanometer

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2014-11
Est. Completion 2017-10
University of California, Irvine

368 total trials

What the finished NCT02527018 record still lists

NCT02527018 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 66 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Sphygmomanometer is the first listed.

NCT02527018 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02527018 about?

NCT02527018 is a clinical study titled "A Comparison of BNP Levels Using the Nexfin Device in Healthy Pregnant and Preeclamptic Women". Primary Endpoint: Quantify the hemodynamic changes in preeclampsia using the non-invasive Nexfin device. Secondary Endpoint: Determine if measurable hemodynamic changes are statistically correlated with B-type natriuretic peptide (BNP) levels.

What is the current status of trial NCT02527018?

This trial is currently completed. The enrollment target is 66 participants. The study started on 2014-11. Estimated completion is 2017-10.

What interventions are being tested in trial NCT02527018?

The interventions under investigation include: Sphygmomanometer (DEVICE).

Who is sponsoring clinical trial NCT02527018?

This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT02527018, the US trial registry maintained by the National Library of Medicine. NCT02527018 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.