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COMPLETED NA

ToothWave Calculus Reduction and Accumulation Prevention Study

NCT04596761 · View on ClinicalTrials.gov ↗

Study Summary

The objective of the study is to evaluate the safety and efficacy of the home-use device ToothWave (Model H7001) for calculus reduction and the prevention of calculus accumulation.

Interventions

  • DEVICE Control placebo with no RF
  • DEVICE RF-utilizing powered toothbrush

Study Locations (1)

Indiana

  • Salus Research — Fort Wayne

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2020-07-15
Est. Completion 2020-12-10
Phase NA

Sponsor

Home Skinovations

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04596761

The ClinicalTrials.gov registry entry for NCT04596761 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 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Home Skinovations, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Gingivitis appearing as the primary indexed condition, and to 2 interventions — of which Control placebo with no RF 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: NCT04596761 reports 1 study location spanning 1 distinct geographic area — top geographies include Indiana. 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 NCT04596761 about?

NCT04596761 is a clinical study titled "ToothWave Calculus Reduction and Accumulation Prevention Study". The objective of the study is to evaluate the safety and efficacy of the home-use device ToothWave (Model H7001) for calculus reduction and the prevention of calculus accumulation.

What is the current status of trial NCT04596761?

This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2020-07-15. Estimated completion is 2020-12-10.

What conditions does trial NCT04596761 study?

This clinical trial studies the following conditions: Gingivitis, Plaque, Calculus, Dental. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04596761?

The interventions under investigation include: Control placebo with no RF (DEVICE), RF-utilizing powered toothbrush (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04596761?

This trial is sponsored by Home Skinovations, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04596761 being conducted?

This trial has 1 study location across Indiana. 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