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Search / Trial NCT00127868

Selenium Sulfide, Ketoconazole and Ciclopirox Shampoo as Additional Treatments for Tinea Capitis (Scalp Ringworm)

Launched by CHEN, CATHERINE, M.D. · Aug 8, 2005

Trial Information

Current as of August 27, 2025

Completed

Keywords

Tinea Capitis Children Pediatric Treatment Therapy Adjunctive Selenium Sulfide Ciclopirox Shampoo

ClinConnect Summary

Antifungal shampoos have been used as supplements to oral griseofulvin to help eradicate tinea capitis (also known as ringworm of the scalp) more quickly. While selenium sulfide shampoo has been the gold standard, its strong odor and its drying effect on the scalp discourage many patients from using it. Meanwhile, no other antifungal shampoo has been rigorously evaluated for efficacy. Therefore, while physicians are prescribing griseofulvin accompanied by any of a number of antifungal shampoos for tinea capitis, it is not known which antifungal shampoos (excluding selenium sulfide) actually...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients with clinically diagnosed tinea capitis.
  • Males or females, ages 1 through 12 years old.
  • Females of childbearing potential must have a negative pregnancy test.
  • Written Informed Consent must be obtained prior to performing any study- related procedure and according to local regulations.
  • Patients must be available for the entire study duration.
  • Exclusion Criteria:
  • Patients who are pregnant or breast-feeding.
  • Patients who have kerions requiring immediate treatment or treatment with systemic corticosteroids and/or systemic antibiotics.
  • Patients who have a skin disease involving the scalp, or any other condition or prior/present treatment which in the opinion of the investigator would interfere with evaluation of the treatment's effect. Examples include head lice, scalp psoriasis, atopic dermatitis of the scalp, or seborrheic dermatitis.
  • Patients with known liver disease.
  • Patients with non-acidic gastroduodenitis, malabsorption syndrome, chronic diarrhea, or any other serious gastrointestinal (GI) disease.
  • Patients who have received systemic antifungal treatment within 2 months prior to baseline.
  • Patients who have received the following topical treatments for their scalp within 1 week prior to baseline: antifungal agents, corticosteroids, zinc pyrithione, selenium sulfide, or tar-containing products.
  • Patients who have received immunosuppressant therapy, cytostatic therapy, or underwent radiation therapy within 1 month prior to baseline.
  • Patients who have been treated with any investigational agent within 8 weeks prior to baseline or who intend to use other investigational treatments during this study.
  • Patients with hypersensitivity to griseofulvin, selenium sulfide, or ciclopirox.
  • Patients who are known to miss appointments (per medical records), unlikely to follow medical instructions, or not willing to attend regular visits.
  • * The following exclusion criteria are based upon the package insert for griseofulvin microsize suspension:
  • Males planning to father children during their participation in the study or in the 6 months following their completion of the study.
  • Patients taking substances known to interact with griseofulvin.
  • Patients with systemic lupus erythematosus.
  • Patients with porphyria.
  • Patients with photosensitivity.

About Chen, Catherine, M.D.

Dr. Catherine Chen, M.D., is a dedicated clinical trial sponsor with extensive expertise in medical research and patient care. With a strong background in clinical medicine and a commitment to advancing healthcare through innovative studies, Dr. Chen leads initiatives that aim to evaluate new treatments and therapies. Her focus on ethical standards and patient safety ensures that all trials are conducted with the highest level of integrity and scientific rigor. Through collaboration with multidisciplinary teams, Dr. Chen strives to contribute meaningful insights to the medical community and improve patient outcomes.

Locations

Norfolk, Virginia, United States

Patients applied

0 patients applied

Trial Officials

Catherine Chen, M.D.

Principal Investigator

Eastern Virginia Medical School

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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