ID

46174

Beschrijving

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.

Link

dbGaP study=phs000263

Trefwoorden

  1. 07-06-22 07-06-22 - Dr. Christian Niklas
  2. 12-10-22 12-10-22 - Adrian Schulz
  3. 29-01-25 29-01-25 - Akane Nishihara
Houder van rechten

Huiying Li, PhD

Geüploaded op

29 januari 2025

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

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dbGaP phs000263 Metagenomic Study of the Human Skin Microbiome Associated with Acne

Eligibility Criteria

Inclusion and exclusion criteria
Beschrijving

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Subjects must:
Beschrijving

Elig.phs000263.v1.p1.1

Datatype

text

Alias
UMLS CUI [1,1]
C1512693
be male or female age 13 or older.
Beschrijving

Elig.phs000263.v1.p1.2

Datatype

text

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0001779
understand the test procedure and must read and sign the appropriate informed consent form indicating their willingness to participate.
Beschrijving

Elig.phs000263.v1.p1.3

Datatype

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C2348563
agree to refrain from using any product on the skin during the study.
Beschrijving

Elig.phs000263.v1.p1.4

Datatype

text

Alias
UMLS CUI [1,1]
C0750484
UMLS CUI [1,2]
C1298908
UMLS CUI [1,3]
C0087111
UMLS CUI [1,4]
C1123023
agree to adhere to the study procedures and requirements.
Beschrijving

Elig.phs000263.v1.p1.5

Datatype

text

Alias
UMLS CUI [1,1]
C0525058
have visible acne lesions on skin, suitable for culture and/or biopsy (for acne patients only).
Beschrijving

Elig.phs000263.v1.p1.6

Datatype

text

Alias
UMLS CUI [1,1]
C2347662
UMLS CUI [1,2]
C0702166
UMLS CUI [1,3]
C0150866
UMLS CUI [1,4]
C0563454
Subjects must not:
Beschrijving

Elig.phs000263.v1.p1.7

Datatype

boolean

Alias
UMLS CUI [1,1]
C0680251
have poor skin condition including erythema, sunburn, abrasions, etc. on the test sites.
Beschrijving

Elig.phs000263.v1.p1.8

Datatype

text

Alias
UMLS CUI [1,1]
C0038814
UMLS CUI [1,2]
C1298908
UMLS CUI [2,1]
C1298908
UMLS CUI [2,2]
C0041834
UMLS CUI [3,1]
C1298908
UMLS CUI [3,2]
C2700379
UMLS CUI [3,3]
C1123023
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.
Beschrijving

Elig.phs000263.v1.p1.9

Datatype

text

Alias
UMLS CUI [1,1]
C1298908
UMLS CUI [1,2]
C0205156
UMLS CUI [1,3]
C2348568
be involved in any aspect of test administration.
Beschrijving

Elig.phs000263.v1.p1.10

Datatype

text

Alias
UMLS CUI [1,1]
C1298908
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C0871511
participate in any other study concurrently which the investigator feels may influence the results of this study.
Beschrijving

Elig.phs000263.v1.p1.11

Datatype

text

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0683954
UMLS CUI [1,4]
C1298908
have any medical condition or factor which the investigator believes might affect the response of the skin.
Beschrijving

Elig.phs000263.v1.p1.12

Datatype

text

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
UMLS CUI [1,4]
C1298908

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000263.v1.p1.1
Item
Subjects must:
text
C1512693 (UMLS CUI [1,1])
Item
be male or female age 13 or older.
text
C0079399 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
Code List
be male or female age 13 or older.
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])
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])
Code List
agree to refrain from using any product on the skin during the study.
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])
Code List
agree to adhere to the study procedures and requirements.
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])
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
C0680251 (UMLS CUI [1,1])
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])
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])
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])
Code List
be involved in any aspect of test administration.
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])
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])
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)

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