OrthoPulse™ Product Evaluation and Assessing Clinical Effectiveness



Status:Recruiting
Conditions:Dental
Therapuetic Areas:Dental / Maxillofacial Surgery
Healthy:No
Age Range:12 - 70
Updated:4/21/2016
Start Date:October 2013
End Date:June 2016
Contact:Darya L Skrenes, B.Sc.
Email:d.skrenes@bioluxresearch.com
Phone:888-669-0674

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The purpose of this investigation is to evaluate the clinical effectiveness of the
OrthoPulse™, an intra-oral LED (Light Emitting Diode) photobiomodulation device, and for
investigators to evaluate the product in a clinical setting.


Inclusion Criteria:

- Eligible and scheduled for full mouth fixed orthodontic treatment or Invisalign

- Non-smoker

- Permanent dentition

- Good oral hygiene, as determined by the investigator orthodontist

Exclusion Criteria:

- Pregnant females

- Patient is currently enrolled in another clinical study

- Periodontally involved teeth

- Use of bisphosphonates (osteoporosis drugs) during the study.

- Patient plans to move over the treatment period
We found this trial at
3
sites
Chandler, Arizona 85224
Principal Investigator: Todd Dickerson, DDS
Phone: 480-963-2535
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New York City, New York 10065
Principal Investigator: Marc Lemchen, DDS
Phone: 212-755-2333
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New York City, NY
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San Antonio, Texas 78232
Principal Investigator: Robert Norris, DDS
Phone: 210-481-7051
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San Antonio, TX
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