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Potential Research Study Participant Registry
This study is currently recruiting participants.
Verified by University of California, Davis, July 2008
First Received: July 2, 2008   No Changes Posted
Sponsored by: University of California, Davis
Information provided by: University of California, Davis
ClinicalTrials.gov Identifier: NCT00710489
  Purpose

The purpose of the potential research study participant registry is to keep potential research subjects informed about any future research studies in which they may meet the criteria for enrollment. The purpose of this study is also to assist current and future clinical trials with recruitment of subjects.


Condition
Acne
Actinic Keratosis
Dysplastic Nevi
Eczema
Psoriasis
Skin Cancer
Rosacea
Leg Ulcers
Foot Ulcers
Atopic Dermatitis

MedlinePlus related topics: Acne Cancer Eczema Foot Health Leg Injuries and Disorders Moles Psoriasis Rosacea Skin Cancer
U.S. FDA Resources
Study Type: Observational
Official Title: Potential Research Study Participant Registry

Further study details as provided by University of California, Davis:

Primary Outcome Measures:
  • Identify Dermatology Clinical research topics of interest in the community. [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 200
Study Start Date: July 2008
Estimated Study Completion Date: January 2010
Estimated Primary Completion Date: January 2009 (Final data collection date for primary outcome measure)
Detailed Description:

Methods:

Subjects will self identify themselves via the UCDMC Dermatology website to complete a survey regarding their interest in learning about future dermatology clinical research projects. Subjects provide contact information and check of a list of potential topics of interest.

Procedures:

Potential participants will find a link on the UCDMC Dermatology website to our registry. The potential participant will read information about the registry. If they wish additional information, they can follow a link to the potential research registry consent form. At this stage, the potential participant may answer, "no" to the consent form and they will be redirected back to the Clinical trials website. If they answer, "yes" then they will be linked to the registry questionnaire. The potential subject would then decide if they want to participate in the registry and if so what information they want to provide. The Clinical Research Coordinators would contact potential study participants to see if they meet the eligibility criteria for any of our current studies.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Adult community members with an interest in one or more of the following dermatologic conditions: Acne, Actinic Keratosis, Blistering Diseases, Dysplastic Nevi (mole), Eczema, Psoriasis, Vitaligo, Skin Cancer Prevention, Skin Cancer Treatment, Phototherapy Treatment Options, Rosacea, Leg or Foot Ulcers, Lichen Planus, Atopic Dermatosis, Canker Sores, others as indicated.

Criteria

Inclusion Criteria:

  • Over 18 years of age

Exclusion Criteria:

  • Under 18 years of age
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00710489

Contacts
Contact: Lucia Rael 916-734-0917 lrael@ucdavis.edu
Contact: Jennifer Nava 916-734-1438 jennifer.nava@ucdmc.ucdavis.edu

Locations
United States, California
University of California, Davis Recruiting
Sacramento, California, United States, 95816
Contact: Lucia Rael     916-734-0917     lrael@ucdavis.edu    
Principal Investigator: Fu-Tong Liu, M.D., Ph.D            
Sponsors and Collaborators
University of California, Davis
Investigators
Principal Investigator: Fu-Tong Liu, M.D., Ph.D. University of California, Davis
  More Information

Additional Information:
No publications provided

Responsible Party: University of California, Davis ( Dr. Fu-Tong Liu, M.D., Ph.D. )
Study ID Numbers: 200815981-1
Study First Received: July 2, 2008
Last Updated: July 2, 2008
ClinicalTrials.gov Identifier: NCT00710489     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, Davis:
Acne
Actinic Keratosis
Dysplastic Nevi
Eczema
Psoriasis
Vitiligo
Skin Cancer
Rosacea
Leg or Foot Ulcers
Atopic Dermatosis

Study placed in the following topic categories:
Keratosis
Dermatitis, Atopic
Eczema
Dysplastic Nevus Syndrome
Foot Diseases
Vitiligo
Acne Vulgaris
Melanoma
Rosacea
Hypersensitivity
Psoriasis
Nevus, Pigmented
Skin Diseases, Eczematous
Skin Diseases, Genetic
Dermatitis
Foot Ulcer
Skin Diseases
Ulcer
Atypical Mole Syndrome
Skin Neoplasms
Neoplastic Syndromes, Hereditary
Genetic Diseases, Inborn
Hypersensitivity, Immediate
Nevus
Skin Ulcer
Skin Diseases, Papulosquamous
Tylosis
Leg Ulcer

Additional relevant MeSH terms:
Keratosis
Dermatitis, Atopic
Eczema
Dysplastic Nevus Syndrome
Foot Diseases
Rosacea
Hypersensitivity
Neoplasms by Site
Pathologic Processes
Psoriasis
Skin Diseases, Eczematous
Nevi and Melanomas
Skin Diseases, Genetic
Dermatitis
Foot Ulcer
Neoplasms by Histologic Type
Skin Diseases
Immune System Diseases
Ulcer
Skin Neoplasms
Neoplasms
Neoplastic Syndromes, Hereditary
Genetic Diseases, Inborn
Hypersensitivity, Immediate
Nevus
Skin Ulcer
Skin Diseases, Papulosquamous
Leg Ulcer

ClinicalTrials.gov processed this record on May 07, 2009