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Potential Research Study Participant Registry

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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00710489
Recruitment Status : Recruiting
First Posted : July 4, 2008
Last Update Posted : July 18, 2017
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
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 or disease
Acne Actinic Keratosis Dysplastic Nevi Eczema Psoriasis Skin Cancer Rosacea Leg Ulcers Foot Ulcers Atopic Dermatitis

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.


Study Design

Study Type : Observational
Estimated Enrollment : 200 participants
Observational Model: Other
Time Perspective: Other
Official Title: Potential Research Study Participant Registry
Study Start Date : May 2008
Estimated Primary Completion Date : January 2025
Estimated Study Completion Date : January 2025

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Groups and Cohorts


Outcome Measures

Primary Outcome Measures :
  1. Identify Dermatology Clinical research topics of interest in the community. [ Time Frame: 2 years ]

Eligibility Criteria

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:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
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

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): NCT00710489


Contacts
Contact: Lam Nguyen 916-734-6556 lam.nguyen@ucdmc.ucdavis.edu

Locations
United States, California
University of California, Davis Recruiting
Sacramento, California, United States, 95816
Contact: Lam Nguyen    916-734-6556    lam.nguyen@ucdmc.ucdavis.edu   
Principal Investigator: Fu-Tong Liu, MD, PhD         
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:
Responsible Party: University of California, Davis
ClinicalTrials.gov Identifier: NCT00710489     History of Changes
Other Study ID Numbers: 200815981
First Posted: July 4, 2008    Key Record Dates
Last Update Posted: July 18, 2017
Last Verified: July 2017

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

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