ClinicalTrials.gg
RecruitingNCT07932470Updated Nov 12, 2026

Fungal Malignant Otitis Externa

An observational study in Fungal Malignant Otitis Externa, sponsored by Sohag University. Recruiting at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2026-11-12.

Sponsored by Sohag University · Observational

From the registry’s dates

  • Started Oct 2026; still recruiting 1 month later.
Updated Nov 12, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
45
Sex
All
01

Study summary

This prospective observational study aims to evaluate the diagnostic and therapeutic challenges of fungal malignant otitis externa in patients attending Sohag University Hospital. It will assess clinical presentation, diagnostic findings, treatment approaches, and clinical outcomes to improve understanding and management of this condition.

02

Conditions studied

  • Fungal Malignant Otitis Externa

Browse trials for

03

In context

Otitis Externa

23 studies on the registry are indexed under Otitis Externa; 2 are open to participants now.

Browse Otitis Externa studies →

Lead sponsor

Sohag University is the lead sponsor of 1,232 studies on the registry; 638 are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients of any age or sex presenting to Sohag University Hospital with suspected or confirmed malignant otitis externa, who will be evaluated clinically and microbiologically to identify fungal pathogens and assess diagnostic and therapeutic challenges.

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

  1. Patients diagnosed or suspected to have malignant otitis externa.
  2. Patients of any age or sex.
  3. Patients willing to participate in the study with appropriate .

Exclusion criteria

Exclusion Criteria:

  1. Patients who refuse to participate in the study.
  2. Patients with incomplete clinical or laboratory data that prevent proper evaluation.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
45 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testCulture and Microbial Identification

    Microbiological culture of appropriate clinical specimens to identify bacterial and fungal pathogens. Further identification and susceptibility testing will be performed when applicable.

06

What researchers measure

Primary outcomes

  1. Number of participants with Clinical, Radiological, and Microbiological Findings in Patients with Fungal Malignant Otitis Externa

    Clinical findings will be assessed by ENT clinical examination. Radiological findings will be assessed using CT and/or MRI. Microbiological findings will be assessed using bacterial and fungal cultures of ear discharge or tissue samples. Results will be reported as the number of patients (n, ) for each finding.

    Time frame: Through study completion, an average of 1 year

07

Study locations

1 of 1 sites recruiting
  • Sohag University Hospital, Sohag University, Sohag, Egypt.
    Sohag, Egypt
    Recruiting
    • Yasmin Adel Hussein, Bachelor of Medicine and Bache · Contactya7953097@gmail.com · +201009966109
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2026 (actual). Primary completion is estimated for Nov 2027, 13 months after the start.

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

Registered
Oct 30, 2026
First posted
Nov 12, 2026
StartActual
Oct 1, 2026
Primary completionEst.
Nov 1, 2027
CompletionEst.
Nov 1, 2027
Last update
Nov 12, 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.
Registered
First appeared on the registry. No changes since
Nov 12, 2026
Show all 1 update
  1. Nov 12, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07932470
Lead sponsor
Sohag University
Responsible party
Yasmin Adel Hussien (Resident Physician, Sohag University) — Principal investigator
First posted
Nov 12, 2026
Start date
Oct 1, 2026
Primary completion
Nov 1, 2027 (estimated)
Completion
Nov 1, 2027 (estimated)
Last update
Nov 12, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion