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COMPLETED NA

Clinical Efficacy Study Comparing VisionScope Imaging (VSI) to Magnetic Resonance Imaging (MRI) in Injuries of the Knee

NCT01695720 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to accumulate efficacy data on VisionScope Imaging (VSI) for pre-operative diagnosis of certain knee injuries (meniscal and articular cartilage injuries). The study will compare VSI's accuracy to MRI's in diagnosing the same injuries. The hypothesis is the VisionScope Imaging system will be able to provide direct visualization and diagnostic images of inside the joint capsule space without fluid distention in the knee. This study will provide valuable feedback on the ability of the VisionScope system to provide physicians with the information they need to make a definitive diagnosis.

Interventions

  • PROCEDURE VisionScope Imaging (VSI) Exam

Study Locations (7)

California

  • Kerlan-Jobe Orthopaedic Foundation — Los Angeles
  • Stanford School of Medicine — Redwood City
  • Santa Monica Orthopaedic & Sports Medicine Group (SMOG) — Santa Monica

Florida

  • Andrews Research and Education Institute — Gulf Breeze

Georgia

  • Emory University Hospital — Atlanta

Texas

  • University of Texas SouthWestern — Dallas

Vermont

  • Mansfield Orthopaedics (Copley Hospital) — Morrisville

Trial Details

FieldValue
Enrollment Target 105 participants
Start Date 2012-06
Est. Completion 2013-05
Phase NA

Sponsor

VisionScope Technologies

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01695720

The ClinicalTrials.gov registry entry for NCT01695720 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is VisionScope Technologies, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Meniscus Tears appearing as the primary indexed condition, and to 1 intervention — of which VisionScope Imaging (VSI) Exam is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01695720 reports 7 study locations spanning 5 distinct geographic areas — top geographies include California, Florida, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01695720 about?

NCT01695720 is a clinical study titled "Clinical Efficacy Study Comparing VisionScope Imaging (VSI) to Magnetic Resonance Imaging (MRI) in Injuries of the Knee". The purpose of the study is to accumulate efficacy data on VisionScope Imaging (VSI) for pre-operative diagnosis of certain knee injuries (meniscal and articular cartilage injuries). The study will compare VSI's accuracy to MRI's in diagnosing the same injuries. The hypothesis is the VisionScope Im...

What is the current status of trial NCT01695720?

This trial is currently completed. It is a NA study. The enrollment target is 105 participants. The study started on 2012-06. Estimated completion is 2013-05.

What conditions does trial NCT01695720 study?

This clinical trial studies the following conditions: Meniscus Tears, Loose Bodies, Articular Osteoarthritis, Articular or Capsular Trauma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01695720?

The interventions under investigation include: VisionScope Imaging (VSI) Exam (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01695720?

This trial is sponsored by VisionScope Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01695720 being conducted?

This trial has 7 study locations across California, Florida, Georgia, Texas, Vermont. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial