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RecruitingNCT07734441Updated Jul 29, 2026

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

An Early Phase 1 interventional study of Itraconazole (200 mg) and Ketoconazole 2% in Seborrheic Dermatitis, sponsored by Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan. Recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-07-29.

Sponsored by Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan · Early Phase 1, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jan 2026, registered Jul 2026).
  • Started Jan 2026; still recruiting 10 months later.
Phase
Early Phase 1
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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). 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.

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.

02

Conditions studied

  • Seborrheic Dermatitis

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Keywords

  • seborrheic dermatitis
  • scalp seborrheic dermatitis
  • moderate to severe disease
03

In context

Dermatitis, Seborrheic

58 studies on the registry are indexed under Dermatitis, Seborrheic; 7 are open to participants now.

This study's planned enrollment of 80 is close to the median of 77 across 47 interventional studies indexed under Dermatitis, Seborrheic.

Browse Dermatitis, Seborrheic studies →

Lead sponsor

Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan is the lead sponsor of 3 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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.
05

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
80 participants (estimated)

Study arms

  • Active comparator
    Oral Itraconazole pulse therapy

    Participants receive oral itraconazole pulse therapy according to the study protocol for medrate to severe seborrheic dermatits

    Drug: Itraconazole (200 mg)

  • Active comparator
    Arm B : Topical 2% ketoconazole shampoo

    Participants receive topical 2% ketoconazole shampoo according to the study protocol for moderate to severe scalp seborrheic dermatitis.

    Drug: Ketoconazole 2%

Interventions

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

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

06

What researchers measure

Primary outcomes

  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.

    Time frame: Baseline and 4 weeks after initiation of treatment.

07

Study locations

1 of 1 sites recruiting
  • CMH Bahawalpur
    Chak Four Hundred Fifty-four, Punjab Province 63100, Pakistan
    Recruiting
    • Bakhtawar Rehman, FCPS Dermatolgy(3.5 years) · Contact03328883135
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2026 (actual). Primary completion is estimated for Sep 2026, 8 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 24, 2026
First posted
Jul 29, 2026
StartActual
Jan 7, 2026
Primary completionEst.
Sep 7, 2026
CompletionEst.
Sep 7, 2026
Last update
Jul 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07734441
Lead sponsor
Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan
Responsible party
Sara Khan (Principal Investigator, Combined Military Hospital (CMH) institute of Medical Sciences Bahawalpur Pakistan) — Principal investigator
First posted
Jul 29, 2026
Start date
Jan 7, 2026
Primary completion
Sep 7, 2026 (estimated)
Completion
Sep 7, 2026 (estimated)
Last update
Jul 29, 2026

Study contacts

Bakhtawar Rehman, MBBS, FCPS Dermatology
Contact
bakhtawar.rehman09@gmail.com
03328883135

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drugs tested here: Itraconazole · Ketoconazole

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