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

NCT01242553 · ClinicalTrials.gov registry record

Clinical Validation Study for iVue

A clinical trial, sponsored by Optovue.

Completed
Registry status
48
Enrollment target

NCT01242553: Completed study, sponsored by Optovue.

NCT01242553 is a clinical trial that has completed, run by Optovue. The registered enrollment target is 48 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01242553 has completed, sponsored by Optovue.

COMPLETED
Registry status
48 participants
Enrollment target

Study Summary

To demonstrate clinical substantial equivalence of iVue as comparable to commercially available RTVue.

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2009-10
Est. Completion 2010-09
Optovue

12 total trials

What the finished NCT01242553 record still lists

NCT01242553 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 48 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT01242553 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01242553 about?

NCT01242553 is a clinical study titled "Clinical Validation Study for iVue". To demonstrate clinical substantial equivalence of iVue as comparable to commercially available RTVue.

What is the current status of trial NCT01242553?

This trial is currently completed. The enrollment target is 48 participants. The study started on 2009-10. Estimated completion is 2010-09.

Who is sponsoring clinical trial NCT01242553?

This trial is sponsored by Optovue, which has 12 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

  • NCT01765777 · 48 participants · NA

    Efficacy of Osteopathic Manipulative Medicine (OMM) and Phototherapy for Patients With Chronic Lower Back Pain

  • NCT03073343 · 48 participants · NA

    A Prospective, Randomized, Open Label Trial of Two Doses of Oral Betaine

  • NCT03431064 · 48 participants

    Lung Recruitment Maneuver as a Potential Predictor of Fluid Responsiveness in Mechanically Ventilated Pediatric Patients

  • NCT03514602 · 48 participants · NA

    Maternal Smoking Cessation and Pediatric Obesity Prevention

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01242553, the US trial registry maintained by the National Library of Medicine. NCT01242553 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.