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Lower Laser Therapy in Orthognathics Surgery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01530100
Recruitment Status : Completed
First Posted : February 9, 2012
Last Update Posted : December 2, 2014
Sponsor:
Information provided by (Responsible Party):
Giovanni Gasperini, Universidade Federal de Goias

Tracking Information
First Submitted Date February 6, 2012
First Posted Date February 9, 2012
Last Update Posted Date December 2, 2014
Study Start Date February 2012
Actual Primary Completion Date April 2013   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: December 1, 2014)
edema, pain and neurosensory disturbancy [ Time Frame: 2 months ]
edema, pain and neurosensory disturbancy, response to lasr therapy
Original Primary Outcome Measures Not Provided
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Lower Laser Therapy in Orthognathics Surgery
Official Title Lower Laser Therapy in Orthognathics Surgery - Double Blind Study.
Brief Summary This study will examine the use of lower laser therapy to reduce edema and pain in orthognathics surgery.
Detailed Description Not Provided
Study Type Observational
Study Design Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Probability Sample
Study Population community sample
Condition Dentofacial Deformity
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: February 8, 2012)
10
Original Estimated Enrollment Same as current
Actual Study Completion Date May 2013
Actual Primary Completion Date April 2013   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Dentofacial deformity
  • Healthy
  • Mandibular surgery
  • no medication use
Sex/Gender
Sexes Eligible for Study: All
Ages Child, Adult, Older Adult
Accepts Healthy Volunteers Yes
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Not Provided
Removed Location Countries  
 
Administrative Information
NCT Number NCT01530100
Other Study ID Numbers LLTOS
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Giovanni Gasperini, Universidade Federal de Goias
Study Sponsor Universidade Federal de Goias
Collaborators Not Provided
Investigators
Principal Investigator: Giovanni Gasperini, master UFG
PRS Account Universidade Federal de Goias
Verification Date February 2012