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Completed

NCT Number: NCT07802808

Effect of 0.75% Piroctone Olamine Shampoo on the Hair and Scalp Microbiota of Hijab-Wearing Women With Seborrheic Dermatitis in Indonesia

The goal of this clinical trial is to learn whether piroctone olamine shampoo works as well as ketoconazole shampoo to improve seborrheic dermatitis (dandruff) in hijab-wearing women in Indonesia. It will also assess the safety of piroctone olamine shampoo. The main questions it aims to answer are:

1. Does piroctone olamine shampoo improve the signs and symptoms of seborrheic dermatitis? 2. Does piroctone olamine shampoo cause any scalp or hair-related side effects?

Researchers will compare piroctone olamine shampoo with ketoconazole shampoo to assess their effects on seborrheic dermatitis.

Participants will:

1. Attend screening and study visits for scalp and hair examinations. 2. Use either piroctone olamine shampoo or ketoconazole shampoo as instructed during the study. 3. Provide hair and scalp samples for microbiota testing and superoxide dismutase testing. 4. Have scalp hydration, water loss, and sebum levels measured. 5. Report any discomfort, scalp irritation, or other side effects during the study.

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Key information

Age range

18 year–59 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

dr. Cipto Mangunkusumo General Hospital

Jakarta, 10430, Indonesia

About this study

The goal of this clinical trial is to learn the effectivity and safety of piroctone olamine shampoo in Hijab-wearing women with seborrheic dermatitis in Indonesia. The main question it aims to answer is:

Does piroctone olamine shampoo improve clinical signs and symptoms of seborrheic dermatitis and demonstrate comparable safety to ketoconazole shampoo in hijab-wearing women with seborrheic dermatitis?

Researchers will compare piroctone olamine shampoo with ketoconazole shampoo to determine whether piroctone olamine shampoo improves seborrheic dermatitis in hijab-wearing women.

Participants will:

  • Be screened to confirm eligibility and provide written informed consent before any study procedures.
  • Undergo baseline assessment of seborrheic dermatitis, including clinical evaluation of the scalp and hair.
  • Provide hair and scalp samples for microbiota analysis and superoxide dismutase level testing
  • Undergo scalp assessments, including skin capacitance, transepidermal water loss (TEWL), and scalp sebum measurements.
  • Be assigned to use either piroctone olamine shampoo or ketoconazole shampoo according to the study instructions.
  • Use the assigned shampoo for the specified treatment duration and follow the scheduled shampoo-use instructions.
  • Attend scheduled follow-up visits for clinical reassessment of seborrheic dermatitis and repeat scalp and hair measurements.
  • Report any discomfort, irritation, allergic reaction, or other adverse events experienced during the study.
  • Complete the final study visit, including final clinical, microbiota, scalp hydration, TEWL, and sebum assessments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hijab-wearing women with mild, moderate, or severe seborrheic dermatitis.
  • Aged 18 to 59 years.
  • Willing to participate in the study and able to provide written informed consent

Exclusion criteria

  • Diagnosis of another hair or scalp condition, such as alopecia, trichotillomania, malignancy, or scalp infection, based on medical history.
  • Current use of medication or treatment for the hair or scalp.
  • Current use of cytostatic therapy for malignancy or other cytostatic medications.
  • Known hypersensitivity to the shampoo base or any of its ingredients, based on medical history.
  • Pregnancy or breastfeeding.
  • Current use of additional hair or scalp-care products.
  • History of liver disease, kidney disease, vitiligo, or psoriasis, based on medical history.

Treatment and study plan

Piroctone Olamine 0.75% Shampoo

Drug

Shampoo containing Piroctone Olamine 0.75%

Ketoconazole Shampoo, 2%

Drug

Ketoconazole shampoo

Primary outcomes

  1. Change in Relative Abundance of Prespecified Hair and Scalp Microbiota

    Time frame: Baseline, Week 2

    Relative abundance of prespecified bacterial and fungal species in hair and scalp samples, including Malassezia restricta, Staphylococcus capitis, and Cutibacterium acnes, will be assessed before and after the intervention. Relative abundance will be compared between participants assigned to 0.75% piroctone olamine shampoo and participants assigned to 2% ketoconazole shampoo.

  2. Change in Seborrheic Dermatitis Severity Measured by the 16-Point Scale

    Time frame: Baseline, Week 2

    Seborrheic dermatitis severity of the hair and scalp will be assessed using the 16-point clinical severity scale. The change in total score from baseline to the follow-up assessment will be compared between the 0.75% piroctone olamine shampoo group and the 2% ketoconazole shampoo group. Higher scores indicate greater clinical severity.

  3. Change in Scalp Skin Capacitance

    Time frame: Baseline, Week 2

    Scalp skin capacitance, an instrumental measure of stratum corneum hydration, will be measured using Corneometer. Change from baseline to the follow-up assessment will be compared between the 0.75% piroctone olamine shampoo group and the 2% ketoconazole shampoo group.

  4. Change in Scalp Transepidermal Water Loss

    Time frame: Baseline, Week 2

    Scalp transepidermal water loss (TEWL) will be measured using Tewameter. Change from baseline to the follow-up assessment will be compared between the 0.75% piroctone olamine shampoo group and the 2% ketoconazole shampoo group.

  5. Change in Scalp Sebum Level

    Time frame: Baseline, Week 2

    Scalp sebum level will be measured using Sebumeter. Change from baseline to the follow-up assessment will be compared between the 0.75% piroctone olamine shampoo group and the 2% ketoconazole shampoo group.

  6. Change in Scalp Superoxide Dismutase (SOD) Level

    Time frame: Baseline, Week 2

    Scalp superoxide dismutase (SOD) level will be measured in scalp samples collected at baseline and at the post-treatment assessment using the prespecified laboratory assay. The change in SOD level from baseline will be compared between participants assigned to 0.75% piroctone olamine shampoo and those assigned to 2% ketoconazole shampoo.

Sponsors and collaborators

Lead sponsor

Indonesia University

Other

Collaborators

  • PT Paragon Technology and Innovation

Registry information

Official study title

Effects of 0.75% Piroctone Olamine Shampoo on Hair and Scalp Microbiota in Hijab-Wearing Women With Seborrheic Dermatitis: A Randomized, Controlled, Double-Blind Clinical Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 3, 2026
Registry last updated
Sep 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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