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NCT04880070 · ClinicalTrials.gov registry record · NA

Post-Market Clinical Follow Up Study to Collect Additional Data and Imaging

A NA study of Connective Tissue Defect, sponsored by Cynosure.

Completed
Registry status
NA
Development phase
5
Enrollment target
1
Study location

NCT04880070 is a NA study of Connective Tissue Defect that has completed, run by Cynosure. The registered enrollment target is 5 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT04880070, a NA study of Connective Tissue Defect, has completed, sponsored by Cynosure.

COMPLETED
Registry status
NA
Development phase
5 participants
Enrollment target
1
Study location

Study Summary

This is a prospective, open label, multi-center clinical study to collect additional data and imaging for the ViaSure device.The intended use of the ViaSure device used in this study is to assess the usability and tissue response to shock wave treatment.

Conditions Studied

Interventions

  • DEVICE Shockwave Treatment

Study Locations (1)

Massachusetts

  • Cynosure, Inc. - Westford

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2021-03-12
Est. Completion 2021-05-11
Phase NA

Sponsor

Cynosure

49 total trials

What the Registry Record Tells You About NCT04880070

The ClinicalTrials.gov registry entry for NCT04880070 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cynosure, which has 49 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Connective Tissue Defect appearing as the primary indexed condition, and to 1 intervention - of which Shockwave Treatment is the first listed.

NCT04880070 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT04880070 about?

NCT04880070 is a clinical study titled "Post-Market Clinical Follow Up Study to Collect Additional Data and Imaging". This is a prospective, open label, multi-center clinical study to collect additional data and imaging for the ViaSure device.The intended use of the ViaSure device used in this study is to assess the usability and tissue response to shock wave treatment.

What is the current status of trial NCT04880070?

This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2021-03-12. Estimated completion is 2021-05-11.

What conditions does trial NCT04880070 study?

This clinical trial studies the following conditions: Connective Tissue Defect.

What interventions are being tested in trial NCT04880070?

The interventions under investigation include: Shockwave Treatment (DEVICE).

Who is sponsoring clinical trial NCT04880070?

This trial is sponsored by Cynosure, which has 49 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04880070 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.