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Seborrheic DermatitisEarly Phase 1NCT07734441

The Effectiveness of Itraconazole Pulse Therapy vs Topical 2% Ketoconazole in the Treatment of Moderate to Severe Seborrheic Dermatitis of Scalp.

A Early Phase 1 study testing Itraconazole (200 mg) and Ketoconazole 2% in people with Seborrheic Dermatitis, run by Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan at 1 site in Pakistan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study is a randomized controlled trial comparing the effectiveness of oral itraconazole pulse therapy versus topical 2% ketoconazole shampoo in treating moderate to severe scalp seborrheic dermatitis (SD). Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Seborrheic Dermatitis
What is being tested?
Itraconazole (200 mg) and Ketoconazole 2%
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 sitePakistan
Study dates
7 Jan 2026to 7 Sep 2026
Phase
Early Phase 1
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients who are interested in taking part in research are between the ages of 14-17 with people who have scalp SD ranging from moderate to severe.

Who cannot join

  • Patients with heart disease. Pregnant women or lactating women liver disease patients as itraconazole can be hepatotoxic uncontrolled hypertension patient taking multiple drugs like oral antidiabetics, lipid lowering drugs, sedatives patient has history to hypersensitvity to either of drugs.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Bakhtawar Rehman, MBBS, FCPS Dermatology contact

03328883135

bakhtawar.rehman09@gmail.com

Pakistan1 site, 1 recruiting
  • CMH Bahawalpur

    Chak Eighty-seven -Twelve Left, Punjab Province, 63100

    Bakhtawar Rehman, FCPS Dermatolgy(3.5 years), 03328883135

    Recruiting

Other trials in Pakistan

About this study

Official title: The Effectiveness of Itraconazole Pulse Therapy vs Topical 2% Ketoconazole in the Treatment of Moderate to Severe Seborrheic Dermatitis of Scalp. A Randomized Control Trial

This study is a randomized controlled trial comparing the effectiveness of oral itraconazole pulse therapy versus topical 2% ketoconazole shampoo in treating moderate to severe scalp seborrheic dermatitis (SD). SD is a chronic inflammatory skin condition associated with Malassezia yeast, characterized by scaling, itching, and redness, significantly affecting quality of life.

A total of 80 participants aged (14-70 years) with moderate to severe scalp SD will be enrolled and divided into two groups. Group A will receive oral itraconazole (pulse regimen over 6 months), while Group B will use ketoconazole shampoo (initial daily use followed by twice weekly application). Outcomes will be assessed using the Scalp Seborrheic Dermatitis (SSD) score, Clinical Global Impression (CGI) scale, and Patient Global Impression (PGI) scale.

Read more

The study aims to compare:

Treatment effectiveness Frequency of disease relapses Patient satisfaction Side-effect profiles Data will be analyzed using statistical tests (t-tests and chi-square), with significance set at p < 0.05.

The hypothesis is that oral itraconazole pulse therapy is more effective than topical ketoconazole in controlling symptoms and preventing relapses in scalp SD.

Read the detailed description

Seborrheic dermatitis (SD) is a chronic, relapsing inflammatory skin disorder that primarily affects sebaceous gland-rich areas such as the scalp, face, chest, and upper back. It presents with greasy scales, erythema, itching, and dandruff, which can significantly impair quality of life. Globally, SD affects approximately 4.38% of the population, with higher prevalence in adults and males.

Although the exact pathogenesis remains unclear, strong evidence highlights the role of Malassezia species in disease development. These yeasts metabolize skin lipids, producing irritant free fatty acids (such as oleic acid), which trigger inflammatory pathways involving cytokines (IL-1β, IL-4, IL-8, IL-17) and NF-kB activation. Microbial imbalance, genetic predisposition (HLA associations), and links with systemic conditions (e.g., HIV, Parkinson's disease, psychiatric disorders) also contribute.

Rationale of the Study Current management focuses on symptom control and prevention of relapses. Antifungal therapies remain the cornerstone of treatment due to the central role of Malassezia.

Topical ketoconazole is widely used and effective but may cause local irritation in some patients.

Oral itraconazole offers both antifungal and anti-inflammatory effects and may provide better long-term control, especially in moderate to severe cases.

However, there is limited comparative evidence between these two approaches in scalp SD. Therefore, this study aims to identify a more effective and practical treatment strategy.

Aim and Objectives The primary aim is to compare oral itraconazole pulse therapy with topical 2% ketoconazole shampoo in managing moderate to severe scalp SD.

Specific objectives include:

Comparing treatment effectiveness Evaluating reduction in disease relapses Assessing patient satisfaction Comparing side-effect profiles Hypothesis Oral itraconazole pulse therapy is more effective than topical ketoconazole shampoo in treating and preventing relapses in moderate to severe scalp SD.

Operational Definitions Severity Measurement: Using the Scalp Seborrheic Dermatitis (SSD) score (0-16), which assesses flaking, erythema, and itching.

Moderate to Severe SD: SSD score >5

Effectiveness: Determined through:

SSD score improvement Clinical Global Impression (CGI) scale (clinician-rated) Patient Global Impression (PGI) scale (patient-reported) Methodology Study Design Randomized Controlled Trial (RCT) Study Setting \& Duration Dermatology OPD, Combined Military Hospital Bahawalpur Duration: 6 months after approval Sample Size Total: 80 patients (40 per group) Calculated using statistical software with 95% confidence level and 80% power, adjusted for dropouts Sampling Technique Non-probability randomized sampling Participants allocated via lottery method Eligibility Criteria

Inclusion Criteria:

Age 14-70 years Moderate to severe scalp SD Willing to participate

Exclusion Criteria:

Cardiac disease Liver disease Pregnancy or lactation Uncontrolled hypertension Polypharmacy (drug interaction risk) Drug hypersensitivity Intervention Groups

Group A (Itraconazole):

100 mg twice daily for 1 week (first month) Then 100 mg twice daily for first 2 days of each month (next 5 months)

Group B (Ketoconazole):

2% shampoo daily for 14 days Then twice weekly for 5 months Data Collection Procedure Baseline data: demographics, disease duration, flare frequency, photographs

Disease severity assessed using SSD score at:

Baseline 3 months 6 months

Final evaluation includes:

CGI score (by blinded dermatologist) PGI score (by patient) Side effects (e.g., nausea, dermatitis, jaundice) recorded throughout Outcome Measures Primary: Improvement in SSD score

Secondary:

CGI and PGI scores Frequency of relapses Side effects Patient satisfaction Data Analysis Plan Software: IBM SPSS 29.0 Descriptive statistics: Mean, standard deviation, etc.

Inferential tests:

Independent t-test (between groups) Paired t-test (within groups) Chi-square test (categorical variables) Statistical significance: p < 0.05 Expected Outcome The study is expected to determine whether oral itraconazole provides superior control of symptoms and relapse prevention compared to topical ketoconazole, potentially offering a more effective treatment strategy for moderate to severe scalp SD.

Being tested
Itraconazole (200 mg), Ketoconazole 2%
Keywords
seborrheic dermatitis, scalp seborrheic dermatitis, moderate to severe disease
Medical subject headings
Dermatitis, Seborrheic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Itraconazole (200 mg)Drug

    Oral itraconazole administered as pulse therapy according to the study protocol.

  • Ketoconazole 2%Drug

    Ketoconazole 2% shampoo applied to the scalp twicw weekly for 4 weeks according to the study protocol.

Study groups in NCT07734441
Study groupRoleWhat they receive
Oral Itraconazole pulse therapyActive comparatorParticipants receive oral itraconazole pulse therapy according to the study protocol for medrate to severe seborrheic dermatits
Receives: Drug: Itraconazole (200 mg)
Arm B : Topical 2% ketoconazole shampooActive comparatorParticipants receive topical 2% ketoconazole shampoo according to the study protocol for moderate to severe scalp seborrheic dermatitis.
Receives: Drug: Ketoconazole 2%

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Seborrheic Dermatitis Severity Score from Baseline

    To compare the effectiveness of itraconazole pulse therapy versus topical 2% ketoconazole shampoo in reducing the severity of moderate to severe scalp seborrheic dermatitis using Seborrheic Dermatitis Severity Score.

    Measured: Baseline and 4 weeks after initiation of treatment.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jul 2026
  2. Study start7 Jan 2026
  3. Primary completion7 Sep 2026 (estimated)
  4. Study completion7 Sep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07734441
Sponsor's protocol ID
1595/EC/14/2025
Status last verified
Apr 2026
First submitted
24 Jul 2026
Last updated
29 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Early Phase 1 study testing Itraconazole (200 mg) and Ketoconazole 2% in people with Seborrheic Dermatitis, run by Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Bakhtawar Rehman, MBBS, FCPS Dermatology (03328883135, bakhtawar.rehman09@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Seborrheic Dermatitis Severity Score from Baseline (time frame: Baseline and 4 weeks after initiation of treatment.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jul 2026.

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