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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.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT01215201
Date of registration: 04/10/2010
Primary sponsor: University of Nebraska
Public title: Diode Laser Study for Periodontal Maintenance Patients
Scientific title: Adjunctive Non-Surgical Therapy of Inflamed Periodontal Pockets Using Diode Lasers During Maintenance Therapy
Date of first enrolment: May 2010
Target sample size: 110
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT01215201
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment  
Countries of recruitment
United States
Contacts
Name:   Naomi-Trang Nguyen, D.D.S.
Address: 
Telephone:
Email:
Affiliation:  University of Nebraska Medical Center, College of Dentistry
Key inclusion & exclusion criteria

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
Health Condition(s) or Problem(s) studied
Periodontal Maintenance Patients With Chronic Periodontitis With =5mm Probing Depth That Have Bleeding on Probing and/or Suppuration.
Intervention(s)
Device: Diode Laser
Primary Outcome(s)
Periodontal clinical parameters [Time Frame: 3 months]
Secondary Outcome(s)
Secondary ID(s)
452-09-EP
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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