Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07217431 · ClinicalTrials.gov registry record

Access BNP Clinical Performance Evaluation: Testing and Clinical Concordance Study

A clinical trial, sponsored by Beckman Coulter.

Completed
Registry status
1,361
Enrollment target

NCT07217431: Completed study, sponsored by Beckman Coulter.

NCT07217431 is a clinical trial that has completed, run by Beckman Coulter. The registered enrollment target is 1,361 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07217431 has completed, sponsored by Beckman Coulter.

COMPLETED
Registry status
1,361 participants
Enrollment target

Study Summary

The goal is to establish clinical performance of a BNP assay on the intended use population and establish clinical concordance on a separate device.

Primary Outcome

Subjects with BNP value above clinical decision point

Interventions

  • DIAGNOSTIC_TEST BNP

Trial Details

FieldValue
Enrollment Target 1,361 participants
Start Date 2024-10-10
Est. Completion 2025-03-25
Beckman Coulter

18 total trials

What the finished NCT07217431 record still lists

NCT07217431 is an observational study that tracks outcomes without assigning an intervention. Its 1,361 participants enrollment target places it among the larger protocols in the corpus.

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

NCT07217431 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07217431 about?

NCT07217431 is a clinical study titled "Access BNP Clinical Performance Evaluation: Testing and Clinical Concordance Study". The goal is to establish clinical performance of a BNP assay on the intended use population and establish clinical concordance on a separate device.

What is the current status of trial NCT07217431?

This trial is currently completed. The enrollment target is 1,361 participants. The study started on 2024-10-10. Estimated completion is 2025-03-25.

What interventions are being tested in trial NCT07217431?

The interventions under investigation include: BNP (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT07217431?

This trial is sponsored by Beckman Coulter, which has 18 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05245227 · 1,358 participants · Phase 3

    Double Simultaneous Uterotonic Agents Versus Single Agent Regimen to Prevent Early Postpartum Hemorrhage

  • NCT02677064 · 1,365 participants

    Identify Barriers to Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Newly Diagnosed and Relapsed Acute Leukemia

  • NCT04489238 · 1,366 participants

    Collection of Information to Better Understand Young Onset Colorectal Cancer

  • NCT07256392 · 1,370 participants · Phase 3

    Long-term Efficacy and Safety Extension (LTE) Study of Barzolvolimab in Participants With Chronic Spontaneous Urticaria

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07217431, the US trial registry maintained by the National Library of Medicine. NCT07217431 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.