Skip to content

The Impact of Baseline Hormonal Profiles (DHEAS, FSH, LH) on Treatment Response to Systemic Isotretinoin in Adult Female Patients With Acne Vulgaris

The Impact of Baseline Hormonal Profiles (DHEAS, FSH, LH) on Treatment Response to Systemic Isotretinoin in Adult Female Patients With Acne Vulgaris

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07818525
Enrollment
64
Registered
2026-09-14
Start date
2026-01-27
Completion date
2027-03-01
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acne Vulgaris

Keywords

acne vulgaris, isotretinoin, androgen, hormone

Brief summary

Acne vulgaris is a common dermatological condition in adult women, often influenced by hormonal factors. Androgens such as dehydroepiandrosterone sulfate (DHEAS) can stimulate sebaceous gland activity, while gonadotropins (FSH and LH) reflect ovarian and hypothalamic-pituitary axis function. Although systemic isotretinoin is highly effective in severe or treatment-resistant acne, variability in treatment response has been observed among female patients. The role of baseline hormonal levels in predicting isotretinoin response remains unclear. Identifying hormonal predictors of treatment response may improve patient stratification and personalized management. Aim of the study is to evaluate whether baseline serum levels of DHEAS, FSH, and LH are associated with clinical response to systemic isotretinoin in women aged 18 years and older with acne vulgaris.

Interventions

None listed

Sponsors

Biruni University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Female patients aged ≥18 years. * Clinical diagnosis of moderate to severe acne vulgaris. * Planned initiation of systemic isotretinoin therapy. * Ability to provide informed consent

Exclusion criteria

* Use of hormonal therapy (oral contraceptives, antiandrogens, systemic corticosteroids) within the last 3 months. * Contraindications to isotretinoin therapy.

Design outcomes

Primary

MeasureTime frameDescription
treatment response of patients with normal and elevated levels of hormonefrom enrollment to the end of treatment at 6 monthsThe number of months and doses during which no new acne breakouts occur after starting isotretinoin treatment will be recorded.

Countries

Turkey (Türkiye)

Contacts

CONTACTÖmer Mert, Specialist Dermatologist MD
omermert95@gmail.com+905396778884

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 15, 2026