We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

DNA of Oral Cytobrush in Three Means Conservation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01038934
First Posted: December 24, 2009
Last Update Posted: December 24, 2009
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.
Information provided by:
UPECLIN HC FM Botucatu Unesp
  Purpose
The aim of this study is to analyze genomic DNA of buccal cytobrush stored in three means conservation.

Condition Intervention Phase
Healthy Procedure: samples collected by buccal cytobrush Early Phase 1

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Evaluation of Genomic DNA of Oral Cytobrush in Three Means Conservation

Further study details as provided by UPECLIN HC FM Botucatu Unesp:

Enrollment: 18
Study Start Date: March 2006
Study Completion Date: December 2009
Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: buccal cytobrhsh
healthy young
Procedure: samples collected by buccal cytobrush

Detailed Description:
Blood samples are an excellent source of large amounts of genomic DNA. However, alternative sources are often needed in epidemiological studies because of difficulties in obtaining blood samples.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years to 33 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • healthy young

Exclusion Criteria:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01038934


Locations
Brazil
School of Dentistry, Sao Paulo State University, Unesp, Araçatuba/SP
Araçatuba, São Paulo, Brazil
Sponsors and Collaborators
UPECLIN HC FM Botucatu Unesp
Investigators
Principal Investigator: Glauco I Miyahara, Professor Univ. Estadual Paulista
  More Information

Responsible Party: Glauco Issamu Miyahara/ Professor, School of Dentistry, Sao Paulo State University, Unesp, Araçatuba/SP
ClinicalTrials.gov Identifier: NCT01038934     History of Changes
Other Study ID Numbers: upeclin/FOA-Unesp-04
First Submitted: December 22, 2009
First Posted: December 24, 2009
Last Update Posted: December 24, 2009
Last Verified: December 2009

Keywords provided by UPECLIN HC FM Botucatu Unesp:
Buccal Mucosa
DNA
Polymerase Chain Reaction