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The Comparative Assessment of Mycological Efficacy, Safety, Recurrence, and Cost-effectiveness of Selenium Sulfide 1.8% Shampoo Versus Ketoconazole 2% Shampoo in Pityriasis Versicolor: a Double-blind Randomized Controlled Trial

Primary Purpose

Pityriasis Versicolor

Status
Completed
Phase
Phase 4
Locations
Indonesia
Study Type
Interventional
Intervention
shampoo with different composition
Sponsored by
Indonesia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pityriasis Versicolor focused on measuring mycological efficacy, ketoconazole, selenium disulfide 1,8%, Pityriasis versicolor

Eligibility Criteria

12 Years - 60 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Having PV characteristic skin lesions,proven by 20% KOH scraping test and Parker Blue-Black® ink, with the founding of short hyphae and group spores or short hyphae only
  • willing to participate in the study by signing the written informed consent
  • Subjects under the age of 18 with permission from parents or guardians.

Exclusion Criteria:

  • A history of hypersensitivity to the ingredients of the shampoo tested.
  • Having skin abnormalities with impaired skin integrity
  • In the treatment of topical anti-fungal therapy for less than two weeks or systemic anti-fungal for less than one month.
  • Pregnancy and breastfeeding.
  • Patients with PV lesions on the face.

Sites / Locations

  • Puskesmas Kecamatan Pulo Gadung

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Selsun Shampoo (SeS2 shampoo)

Ketoconazole shampoo

Arm Description

Subject were given the SeS2 1.8% shampoo for 2 weeks. They should use it everyday, 10ml each time for 10 minutes. Evaluation was weekly and note for side effects and compliance

Subject were given the Ketoconazole 2% shampoo for 2 weeks. They should use it everyday, 10ml each time for 10 minutes. Evaluation was weekly and note for side effects and compliance

Outcomes

Primary Outcome Measures

mycology efficacy
skin scrapping with KOH test 20% and Parker Blue-Black® ink with the founding of short hyphae and group spores or short hypha only as a positive result
mycology efficacy
skin scrapping with KOH test 20% and Parker Blue-Black® ink with the founding of short hyphae and group spores or short hypha only as a positive result
compliance
the number of day in which a participant using the shampoo which was assigned for minimum 5 days or more and the remaining volume of shampoo does not exceed 25 ml.
compliance
the number of day in which a participant using the shampoo which was assigned for minimum 5 days or more and the remaining volume of shampoo does not exceed 25 ml.
side effect
based on clinical symptoms : itching, burning or stinging sensation. Assessed based on patient records in the diary and through interviews during control
side effect
based on clinical symptoms : itching, burning or stinging sensation. Assessed based on patient records in the diary and through interviews during control
cost-effectiveness
Cost calculations include administrative fees (registration and consultation of doctors), laboratory examinations, medical expenses and compensation for side effects adjusted for the duration of therapy. The results of the calculation of costs obtained are then linked to the negative outcome difference (KOH is still positive) or the value of absolute risk reduction (ARR) on day 14. So that cost efficacy is seen from Incremental Cost-Effectiveness Ratio
recurrence
if the KOH test 20% give a positive result again

Secondary Outcome Measures

Full Information

First Posted
June 15, 2019
Last Updated
July 2, 2019
Sponsor
Indonesia University
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1. Study Identification

Unique Protocol Identification Number
NCT04007237
Brief Title
The Comparative Assessment of Mycological Efficacy, Safety, Recurrence, and Cost-effectiveness of Selenium Sulfide 1.8% Shampoo Versus Ketoconazole 2% Shampoo in Pityriasis Versicolor: a Double-blind Randomized Controlled Trial
Official Title
The Comparative Assessment of Mycological Efficacy, Safety, Recurrence, and Cost-effectiveness of Selenium Sulfide 1.8% Shampoo Versus Ketoconazole 2% Shampoo in Pityriasis Versicolor: a Double-blind Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
September 1, 2018 (Actual)
Primary Completion Date
December 30, 2018 (Actual)
Study Completion Date
December 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indonesia University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
There are several topical treatment for Pityriasis Versicolor including ketoconazole and selenium sulfide. Ketoconazole is a broad spectrum anti-fungal drug from imidazole group that has been reported to be effective in PV. The study aimed to reveal the mycological efficacy, safety, recurrence and cost-effectiveness of selenium sulfide 1.8% shampoo (SeS2) and ketoconazole 2% shampoo in the treatment of pityriasis versicolor. A double blind randomized controlled trial was performed in patients with PV during September-December 2018. Patients who involved in this study were allocated to SeS2 or ketoconazole 2% based on block randomization. Physical examinations, scale provocation test, Wood lamp and potassium hydroxide (KOH) examination were conducted to evaluate the treatment response and side effects on 7th - 14th day. Intention to treat analysis was performed in this study. cost-effectiveness was analyzed by Incremental Cost-Effectiveness Ratio (ICER).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pityriasis Versicolor
Keywords
mycological efficacy, ketoconazole, selenium disulfide 1,8%, Pityriasis versicolor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Masking Description
double blind randomized clinical trial
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Selsun Shampoo (SeS2 shampoo)
Arm Type
Experimental
Arm Description
Subject were given the SeS2 1.8% shampoo for 2 weeks. They should use it everyday, 10ml each time for 10 minutes. Evaluation was weekly and note for side effects and compliance
Arm Title
Ketoconazole shampoo
Arm Type
Active Comparator
Arm Description
Subject were given the Ketoconazole 2% shampoo for 2 weeks. They should use it everyday, 10ml each time for 10 minutes. Evaluation was weekly and note for side effects and compliance
Intervention Type
Drug
Intervention Name(s)
shampoo with different composition
Intervention Description
To reveal the mycological efficacy, safety, recurrence and cost-effectiveness of selenium sulfide 1.8% shampoo (SeS2) and ketoconazole 2% shampoo in the treatment of pityriasis versicolor.
Primary Outcome Measure Information:
Title
mycology efficacy
Description
skin scrapping with KOH test 20% and Parker Blue-Black® ink with the founding of short hyphae and group spores or short hypha only as a positive result
Time Frame
7 days
Title
mycology efficacy
Description
skin scrapping with KOH test 20% and Parker Blue-Black® ink with the founding of short hyphae and group spores or short hypha only as a positive result
Time Frame
14 days
Title
compliance
Description
the number of day in which a participant using the shampoo which was assigned for minimum 5 days or more and the remaining volume of shampoo does not exceed 25 ml.
Time Frame
7 days
Title
compliance
Description
the number of day in which a participant using the shampoo which was assigned for minimum 5 days or more and the remaining volume of shampoo does not exceed 25 ml.
Time Frame
14 days
Title
side effect
Description
based on clinical symptoms : itching, burning or stinging sensation. Assessed based on patient records in the diary and through interviews during control
Time Frame
7 days
Title
side effect
Description
based on clinical symptoms : itching, burning or stinging sensation. Assessed based on patient records in the diary and through interviews during control
Time Frame
14 days
Title
cost-effectiveness
Description
Cost calculations include administrative fees (registration and consultation of doctors), laboratory examinations, medical expenses and compensation for side effects adjusted for the duration of therapy. The results of the calculation of costs obtained are then linked to the negative outcome difference (KOH is still positive) or the value of absolute risk reduction (ARR) on day 14. So that cost efficacy is seen from Incremental Cost-Effectiveness Ratio
Time Frame
two weeks
Title
recurrence
Description
if the KOH test 20% give a positive result again
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Having PV characteristic skin lesions,proven by 20% KOH scraping test and Parker Blue-Black® ink, with the founding of short hyphae and group spores or short hyphae only willing to participate in the study by signing the written informed consent Subjects under the age of 18 with permission from parents or guardians. Exclusion Criteria: A history of hypersensitivity to the ingredients of the shampoo tested. Having skin abnormalities with impaired skin integrity In the treatment of topical anti-fungal therapy for less than two weeks or systemic anti-fungal for less than one month. Pregnancy and breastfeeding. Patients with PV lesions on the face.
Facility Information:
Facility Name
Puskesmas Kecamatan Pulo Gadung
City
Jakarta
Country
Indonesia

12. IPD Sharing Statement

Learn more about this trial

The Comparative Assessment of Mycological Efficacy, Safety, Recurrence, and Cost-effectiveness of Selenium Sulfide 1.8% Shampoo Versus Ketoconazole 2% Shampoo in Pityriasis Versicolor: a Double-blind Randomized Controlled Trial

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