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

NCT00127868 | Completed

• 1 other identifier: 1-Chen
• Study Type: interventional
• Target: 47
• Locations: 1 country
• Sites: 1

Brief 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 significantly reduce time to cure, nor which do so the fastest. Scalp ringworm can also re-occur in the same child. To date, no studies have been done to find out whether or not the use of antifungal shampoos can prevent the recurrence of scalp ringworm. In this study, children ages 1-12 years old, who have clinically diagnosed tinea capitis, will all be prescribed oral griseofulvin for 8 weeks. In addition, they will be randomly assigned to use either selenium sulfide shampoo, ketoconazole shampoo, ciclopirox shampoo, or baby shampoo twice a week for 8 weeks. After 8 weeks, griseofulvin will be stopped. All patients will continue using the same assigned shampoo twice weekly for 24 weeks, while continuing to return to clinic every 4 weeks for scalp evaluation.

Conditions

Tinea Capitis

Keywords

Tinea Capitis; Children; Pediatric; Treatment; Therapy; Adjunctive; Selenium Sulfide; Ciclopirox; Shampoo

Outcome Measures

Primary Outcomes (1)

• efficacy

  9-10 months

Study Arms (4)

1

ACTIVE COMPARATOR

oral griseofulvin and selenium sulfide shampoo 1%

Drug: oral griseofulvin, selenium sulfide shampoo 1%, ciclopirox shampoo , ketoconazole shampoo 2%, baby shampoo

2

ACTIVE COMPARATOR

oral griseofulvin and ciclopirox shampoo

Drug: oral griseofulvin, selenium sulfide shampoo 1%, ciclopirox shampoo , ketoconazole shampoo 2%, baby shampoo

3

ACTIVE COMPARATOR

oral griseofulvin and ketoconazole shampoo 2%

Drug: oral griseofulvin, selenium sulfide shampoo 1%, ciclopirox shampoo , ketoconazole shampoo 2%, baby shampoo

4

PLACEBO COMPARATOR

oral griseofulvin and baby shampoo

Drug: oral griseofulvin, selenium sulfide shampoo 1%, ciclopirox shampoo , ketoconazole shampoo 2%, baby shampoo

Interventions

oral griseofulvin, selenium sulfide shampoo 1%, ciclopirox shampoo , ketoconazole shampoo 2%, baby shampoo DRUG

1; 2; 3; 4

Eligibility Criteria

• Age: 12 Months - 12 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• 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.

You may not qualify if:

• 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.
• 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.

Sponsors & Collaborators

• Chen, Catherine, M.D.: lead
• Williams, Judith V., M.D.: collaborator
• Hubbard, Thomas W., M.D.: collaborator
• Eastern Virginia Medical School: collaborator

Study Sites (1)

Children's Hospital of the King's Daughters

Norfolk, Virginia, 23507, United States

Location

MeSH Terms

Conditions

Tinea Capitis

Interventions

Griseofulvin

Condition Hierarchy (Ancestors)

Tinea; Dermatomycoses; Mycoses; Bacterial Infections and Mycoses; Infections; Skin Diseases, Infectious; Scalp Dermatoses; Skin Diseases; Skin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Benzofurans; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds

Study Officials

• Catherine Chen, M.D.

  Eastern Virginia Medical School

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER

Study Record Dates

• First Submitted: August 5, 2005
• First Posted: August 9, 2005
• Study Start: March 1, 2005
• Primary Completion: April 1, 2008
• Study Completion: April 1, 2008
• Last Updated: July 9, 2008

Record last verified: 2006-05

Locations

US (1)