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Tracking Information | |||||
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First Received Date † | June 2, 2008 | ||||
Last Updated Date | June 10, 2008 | ||||
Start Date † | April 2007 | ||||
Current Primary Outcome Measures † |
Observe comparators of African American and Caucasian women's hair [ Time Frame: 3 days ] [ Designated as safety issue: No ] | ||||
Original Primary Outcome Measures † | Same as current | ||||
Change History | Complete list of historical versions of study NCT00690664 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures † | |||||
Original Secondary Outcome Measures † | |||||
Descriptive Information | |||||
Brief Title † | Evaluation of Scalp and Hair Shaft With Biologic Markers in African American and Caucasian Hair | ||||
Official Title † | Evaluation of Scalp and Hair Shaft With Biologic Markers in African American and Caucasian Hair | ||||
Brief Summary | The purpose of this research study is to better understand African American hair and scalp, its biologic appearance and how this relates to African Americans' perceptions of their hair and scalp health. Since most hair studies have looked at Caucasian hair and scalp, we will use a population of Caucasian subjects for comparison in evaluating various hair and scalp parameters. |
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Detailed Description | |||||
Study Phase | |||||
Study Type † | Observational | ||||
Study Design † | Case Control, Prospective | ||||
Condition † | Scalp Health | ||||
Intervention † | |||||
Study Arms / Comparison Groups |
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Publications * | |||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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Recruitment Information | |||||
Recruitment Status † | Active, not recruiting | ||||
Estimated Enrollment † | 60 | ||||
Estimated Completion Date | September 2008 | ||||
Primary Completion Date | May 2008 (final data collection date for primary outcome measure) | ||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Female | ||||
Ages | 21 Years to 60 Years | ||||
Accepts Healthy Volunteers | Yes | ||||
Contacts †† | |||||
Location Countries † | United States | ||||
Expanded Access Status | |||||
Administrative Information | |||||
NCT ID † | NCT00690664 | ||||
Responsible Party | Amy McMichael, MD, Wake Forest University Health Sciences | ||||
Secondary IDs †† | 31716 | ||||
Study Sponsor † | Wake Forest University | ||||
Collaborators †† | |||||
Investigators † |
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Information Provided By | Wake Forest University | ||||
Verification Date | June 2008 | ||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |