Examining the link between telomere length and skin aging
Association of Leucocyte Telomere Length With Clinical Examination and Dermoscopic Photoaging Scale (DPAS) Score in Skin Aging: a Pilot Study
This study is testing whether measuring telomere length in blood can help us understand how skin ages in people between 29-31 and 59-61 years old.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 29 Years to 61 Years |
| Sex | All |
| Sponsor | Indonesia University Academic / other |
| Locations | 1 site (Jakarta Pusat, DKI Jakarta) |
| Trial ID | NCT06501547 on ClinicalTrials.gov |
What this trial studies
This study aims to investigate the relationship between leucocyte telomere length and the Dermoscopic Photoaging Scale (DPAS) in assessing skin aging. Participants aged 29-31 and 59-61 will undergo clinical examinations by dermatovenereologists, including dermoscopy of specific facial regions and blood draws to measure telomere length. The study seeks to profile photoaging through clinical assessments and telomere analysis, providing insights into the biological markers of skin aging.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy males and females aged 29-31 and 59-61 who exhibit signs of skin aging.
Not a fit: Patients who are pregnant, breastfeeding, or have underlying diseases or genetic problems may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of skin aging and lead to improved assessment and treatment strategies for age-related skin conditions.
How similar studies have performed: While the specific combination of telomere length and DPAS in skin aging is novel, related studies have shown promise in understanding the biological aspects of aging.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female and Male (age 29-31 years old and 59-61 years old * signs of aging Exclusion Criteria: * pregnant or breastfeeding * have disease or genetic problem
Where this trial is running
Jakarta Pusat, DKI Jakarta
- Universitas Indonesia — Jakarta Pusat, DKI Jakarta, Indonesia (Recruiting)
Study contacts
- Study coordinator: Irma Bernadette Sitohang, Prof
- Email: irma_bernadette@yahoo.com
- Phone: +62818130761
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.