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Informations:
Erreur:
ID
45266
Description
Principal Investigator: Huiying Li, PhD, David Geffen School of Medicine, University of California, Los Angeles, CA, USA MeSH: Acne Vulgaris https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000263 Acne vulgaris affects 17 million Americans, more than 80% of the people of age 12-24. The goal of this study is to investigate the relationship between acne pathogenesis and the skin microbiota residing in the microcomedones. This study will enroll approximately 100 healthy individuals and acne patients, both male and female with age 13 or older. Data obtained from this study will help better understand the disease pathogenesis and may lead to the development of new effective therapeutic strategies for treatment of acne.
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Mots-clés
Versions (3)
- 07/06/2022 07/06/2022 - Dr. Christian Niklas
- 12/10/2022 12/10/2022 - Adrian Schulz
- 29/01/2025 29/01/2025 - Akane Nishihara
Détendeur de droits
Huiying Li, PhD
Téléchargé le
12 octobre 2022
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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dbGaP phs000263 Metagenomic Study of the Human Skin Microbiome Associated with Acne
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Case or control status, gender, and ethnicity of subjects affected or not effected with acne.
- The phenotype of samples in association with subject's age, case or control status, acne lesion, acne treatment, and cosmetic procedures.
- Subject ID, consent group, and case or control status of participants affected or not affected with acne.
- Sample ID and subject ID of participants affected or not affected with acne.
- Sample ID and Trace ID of participants affected or not affected with acne.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Case or control status, gender, and ethnicity of subjects affected or not effected with acne.
- The phenotype of samples in association with subject's age, case or control status, acne lesion, acne treatment, and cosmetic procedures.
- Subject ID, consent group, and case or control status of participants affected or not affected with acne.
- Sample ID and subject ID of participants affected or not affected with acne.
- Sample ID and Trace ID of participants affected or not affected with acne.
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0680251 (UMLS CUI [1,2])
Elig.phs000263.v1.p1.1
Item
Subjects must:
text
Item
be male or female age 13 or older.
text
C0079399 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,2])
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Item
understand the test procedure and must read and sign the appropriate informed consent form indicating their willingness to participate.
text
C0021430 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C0162340 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
Code List
understand the test procedure and must read and sign the appropriate informed consent form indicating their willingness to participate.
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Item
agree to refrain from using any product on the skin during the study.
text
C0750484 (UMLS CUI [1,1])
C1298908 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1123023 (UMLS CUI [1,4])
C1298908 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1123023 (UMLS CUI [1,4])
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Item
agree to adhere to the study procedures and requirements.
text
C0525058 (UMLS CUI [1,1])
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Item
have visible acne lesions on skin, suitable for culture and/or biopsy (for acne patients only).
text
C2347662 (UMLS CUI [1,1])
C0702166 (UMLS CUI [1,2])
C0150866 (UMLS CUI [1,3])
C0563454 (UMLS CUI [1,4])
C0702166 (UMLS CUI [1,2])
C0150866 (UMLS CUI [1,3])
C0563454 (UMLS CUI [1,4])
Code List
have visible acne lesions on skin, suitable for culture and/or biopsy (for acne patients only).
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Elig.phs000263.v1.p1.7
Item
Subjects must not:
boolean
Item
have poor skin condition including erythema, sunburn, abrasions, etc. on the test sites.
text
C0038814 (UMLS CUI [1,1])
C1298908 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2,1])
C0041834 (UMLS CUI [2,2])
C1298908 (UMLS CUI [3,1])
C2700379 (UMLS CUI [3,2])
C1123023 (UMLS CUI [3,3])
C1298908 (UMLS CUI [1,2])
C1298908 (UMLS CUI [2,1])
C0041834 (UMLS CUI [2,2])
C1298908 (UMLS CUI [3,1])
C2700379 (UMLS CUI [3,2])
C1123023 (UMLS CUI [3,3])
Code List
have poor skin condition including erythema, sunburn, abrasions, etc. on the test sites.
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Item
have participated in a study wherein the test areas were previously indicated as test sites within one month prior to the start date of this study.
text
C1298908 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0205156 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
Code List
have participated in a study wherein the test areas were previously indicated as test sites within one month prior to the start date of this study.
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Item
be involved in any aspect of test administration.
text
C1298908 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C0871511 (UMLS CUI [1,3])
C1314939 (UMLS CUI [1,2])
C0871511 (UMLS CUI [1,3])
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)
Elig.phs000263.v1.p1.11
Item
participate in any other study concurrently which the investigator feels may influence the results of this study.
text
C2348568 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C1298908 (UMLS CUI [1,4])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C1298908 (UMLS CUI [1,4])
Item
have any medical condition or factor which the investigator believes might affect the response of the skin.
text
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C1298908 (UMLS CUI [1,4])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C1298908 (UMLS CUI [1,4])
Code List
have any medical condition or factor which the investigator believes might affect the response of the skin.
CL Item
No (0)
CL Item
Yes (1)
CL Item
No answer (2)