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Profiles Analysis of Genome Wide Association Study (GWAS) in Acne Vulgaris in Indonesia.

D

Dr.dr.Irma Bernadette, SpKK (K)

Status

Enrolling

Conditions

Acne Vulgaris

Treatments

Genetic: GWAS

Study type

Interventional

Funder types

Other

Identifiers

NCT06501560
Univ_Indo

Details and patient eligibility

About

This study is a series of descriptive-analytic studies on genomic variants in the facial skin of patients with AV at the Dermatology and Venereology Polyclinic by determining the genetic profile by GWAS examination in AVB and analysing the genetic profile in AVB against differences in geographical location. The research design used was a cross-sectional design.

Full description

Research subjects were obtained from the affordable population who met the research criteria and expressed their willingness to participate in the study.

Subject selection was carried out by purposive sampling method that met the inclusion criteria. The study will be conducted in one visit where the patient and his/her parents come to be given an explanation about the study with a request for informed consent, screening for inclusion and exclusion criteria, anamnesis of facial complaints, taking data on demographics, patient's medical history, patient's medical history, physical examination, taking clinical photos in 5 positions and ending with taking blood samples of the patient and blood samples from both parents of the patient as much as 10 mL.

The study will be conducted in three places, namely in Jakarta, Padang, and Manado. In sampling in Padang and Manado, to prevent damage to the samples that have been taken, the samples will be stored at a temperature of -20C, then when brought to Jakarta will use a cooler box along with an ice pack at a temperature of 2-3C, before being processed in the Bioinformatics Core Facilities IMERI laboratory, Jakarta. When the samples are collected in Jakarta, the blood samples will be immediately stored in the laboratory at -20C.

Enrollment

24 estimated patients

Sex

All

Ages

17 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Males or females with AVB aged 17-21 years
  • Both parents of complete subjects with or without a history of acne vulgaris aged up to 60 years
  • Patients and parents are willing to participate in the study and sign informed consent.

Exclusion criteria

  • Patients who have other inflammatory or infectious diseases especially on the face
  • Have genetic diseases or disorders
  • Diagnosed with primary or secondary immunodeficiency diseases
  • Using oral or systemic antibiotic, anti-inflammatory, retinoid or hormone therapy in the past month.

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

Lifestyle counseling
Experimental group
Treatment:
Genetic: GWAS
clinical examination
Experimental group
Treatment:
Genetic: GWAS

Trial contacts and locations

1

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Central trial contact

Irma Bernadette, Professor

Data sourced from clinicaltrials.gov

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