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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01215201 |
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Date of registration:
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04/10/2010 |
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Primary sponsor: |
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Public title:
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Diode Laser Study for Periodontal Maintenance Patients
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Scientific title:
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Adjunctive Non-Surgical Therapy of Inflamed Periodontal Pockets Using Diode Lasers During Maintenance Therapy |
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Date of first enrolment:
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May 2010 |
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Target sample size:
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110 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01215201 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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Countries of recruitment
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United States
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Contacts
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Name:
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Naomi-Trang Nguyen, D.D.S. |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Nebraska Medical Center, College of Dentistry |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Any adult periodontal maintenance patient having had chronic periodontitis with last active therapy at least 3 months prior and with 1 or more sites/subject with =5mm probing depth that have bleeding on probing and/or suppuration. They have signed an informed consent form to participate in the study.
Exclusion Criteria:
- Subjects who are un-controlled diabetics, use NSAIDS regularly for chronic disease/pain, used antibiotics for the last 3 months, require antibiotic coverage for therapy, are pregnant and below age 30.
Age minimum:
30 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Periodontal Maintenance Patients With Chronic Periodontitis With =5mm Probing Depth That Have Bleeding on Probing and/or Suppuration.
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Intervention(s)
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Device: Diode Laser
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Primary Outcome(s)
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Periodontal clinical parameters
[Time Frame: 3 months]
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Secondary ID(s)
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452-09-EP
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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