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Dermatophyte InfectionNCT06729216

Fungal Resistance in Dermatophyte Infection

An observational study of Dermatophyte Infection, run by Cairo University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

The aim of the study is to compare the efficiency of broth microdilution versus disk diffusion method for antifungal drug susceptibility testing of the most used drugs in dermatophytosis treatment. Read more about this study

Who is it for?
Any age
Conditions the study is for
Dermatophyte Infection
What is being tested?
Antifungal susceptibility testing (AFST)
How many people
42 participants
Where
No sites listed yet
Study dates
1 Jun 2025to 1 Aug 2025
Phase
Observational
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 Any age
  • All sexes
  • Child, Adult, Older adult

Study population: Patients with dermatophytic skin infection

Who may be able to join

  • Patients diagnosed clinically with dermatophytosis, any age group and any sex

Who cannot join

  • Patients under either Local or systemic antifungal treatment

About this study

Official title: Species Identification and Antifungal Susceptibility Testing of Dermatophytes Isolated From Patients Attending Dermatology Outpatient Clinic at Kasr Alainy Hospitals

The aim of the study is to compare the efficiency of broth microdilution versus disk diffusion method for antifungal drug susceptibility testing of the most used drugs in dermatophytosis treatment.

Being tested
Antifungal susceptibility testing (AFST)
Medical subject headings
Dermatomycoses

What participants receive

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

  • Antifungal susceptibility testing (AFST)Diagnostic test

    testing the fungal susceptibility to different drugs

Study groups in NCT06729216
Study groupRoleWhat they receive
Antifungal susceptibility testing (AFST)Not described
Receives: Diagnostic Test: Antifungal susceptibility testing (AFST)

What is being measured

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

  1. Precent susceptibility to each drug

    Measure the area of inhibition zone of the drugs to the fungus on the culture

    Measured: 3 months

Timeline

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

  1. First posted11 Dec 2024
  2. Study start1 Jun 2025 (estimated)
  3. Primary completion1 Jul 2025 (estimated)
  4. Study completion1 Aug 2025 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case only
Time perspective
Cross-sectional
Enrolment
42 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06729216
Sponsor's protocol ID
Cutaneous Fungal resistance
Status last verified
May 2025
First submitted
8 Dec 2024
Last updated
14 May 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Dermatophyte Infection, run by Cairo University.

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: opening soon, as of the sponsor's last update on 14 May 2025. Status can change between updates, so confirm with the study contact before making plans.

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.

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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Precent susceptibility to each drug (time frame: 3 months). 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 14 May 2025.

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