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Clinical Trials/NCT04551612
NCT04551612UnknownNot Applicable

Evaluation of the Level of Middle Cranial Fossa Dura in Patients With Cholesteatoma

Assiut University0 sites80 target enrollmentStarted: October 1, 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
80
Primary Endpoint
Evaluation of the Level of Middle Cranial Fossa Dura in Patients with Cholesteatoma by multislice computed tomography.

Study Overview

Brief Summary

Cholesteatoma is a destructive lesion that progressively expands in the middle ear, mastoid or petrous bone and leads to destruction of the nearby structures. Erosion, which is caused by bone resorption of the ossicular chain and otic capsule, may cause hearing loss, vestibular dysfunction, facial paralysis and intracranial manifestations

Detailed Description

Cholesteatoma has three Classical forms: (1) Congenital, primary or genuine cholesteatoma: occurs behind an intact tympanic membrane. Primary acquired cholesteatoma: looks like a limited diverticulum of the pars flaccida with little or no history of otorrhea. Secondary acquired cholesteatoma: develops with posterosuperior perforations in eardrum and expansion of the disease process into the antrum, mastoid, attic and middle ear. Granulation tissue, polyps and foul- smelling otorrhea are common findings in this type

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All adults above the age of 18 presented to the Assiut university Clinic with
  • cholesteatoma will be included in the study.

Exclusion Criteria

  • Patients with previous mastoid surgery
  • Patients with Craniofacial anomalies or cleft lip and palate
  • Pediatric populations ≤ 18 years old
  • Patients with congenital ear anomalies

Outcomes

Primary Outcomes

Evaluation of the Level of Middle Cranial Fossa Dura in Patients with Cholesteatoma by multislice computed tomography.

Time Frame: One year

determination the level of tegmen in patients with attico-antral diseases by MSCT

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mariam Zakaria

Principal investigator

Assiut University

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