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Status unknownNCT03469427Updated Jul 6, 2018

Multislice Computed Tomography in Cases With Facial Nerve Paralysis Due to Temporal Bone Trauma

An observational study in Facial Nerve Paralysis, sponsored by Assiut University. Status unknown at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2018-07-06.

Sponsored by Assiut University · Observational

The sponsor has not verified this record recently (last verified Jul 2018), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
15
Sex
All
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Study summary

Facial nerve paralysis is a disfiguring complication which occurs in 7-10 % of temporal bone fractures.

The onset of paralysis may be immediate, delayed or undetermined, the latter of which often occurs in unconscious patients with accompanying life-threatening complications.About one fourth has complete paralysis.

Read the detailed description

Facial nerve paralysis might have variable etiologies apart from idiopathic Bell's palsy, Congenital, infectious, inflammatory, neoplastic, neurological, toxic, iatrogenic and atraumatic causes.

Surgical intervention is indicated if 90-95% loss of function is seen at the very early period on Electroneuronography or if there is axonal degeneration on Electromyography lately with no sign of recovery.

High-resolution multislice computed tomography of the temporal bone is routinely required for evaluation of traumatic facial paralysis. High-resolution multislice computed tomography is known to be the best method for evaluating the intratemporal course of the facial nerve, but it has some limitations as well. Occasionally, the surgeon may encounter facial nerve injuries which have not been revealed in the preoperative computed tomography.

There are limited data in recent medical publications evaluating the diagnostic value of temporal bone High-resolution multislice computed tomography in the evaluation of traumatic facial paralysis. Therefore, in this study,the investigators will compare the findings of preoperative high-resolution multislice computed tomography with surgical findings to determine the diagnostic value of computed tomography.

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Conditions studied

  • Facial Nerve Paralysis

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03

In context

Bell Palsy

85 studies on the registry are indexed under Bell Palsy; 30 are open to participants now.

This study's planned enrollment of 15 is below the median of 80 across 13 observational studies indexed under Bell Palsy.

Browse Bell Palsy studies →

Lead sponsor

Assiut University is the lead sponsor of 5,079 studies on the registry; 2,177 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

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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 different age groups presented with facial nerve paralysis due to temporal bone trauma

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

  • All patients with temporal bone fracture presented with facial nerve paralysis of immediate onset and meet the criteria of facial nerve exploration regardless of age and sex.

Exclusion criteria

Exclusion Criteria:

  • Pregnant women.
  • Unfit patients for surgery.
  • Patients refuse surgical intervention.
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
15 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Patients who suffer from facial nerve paralysis due to temporal bone trauma will be diagnosed by using multislice computed tomography

    Evaluation the reliability of multislice computed tomography in the assessment of facial nerve paralysis due to temporal bone trauma

    Time frame: up to 2 years

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Study locations

1 of 1 sites recruiting
  • Assiut university hospital
    Assiut, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started May 2018 (actual). Primary completion is estimated for Nov 2019, 18 months after the start.

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

Registered
Mar 12, 2018
First posted
Mar 19, 2018
StartActual
May 1, 2018
Primary completionEst.
Nov 1, 2019
CompletionEst.
Feb 1, 2020
Last update
Jul 6, 2018
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 6, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03469427
Lead sponsor
Assiut University
Responsible party
Sally S Hanna (principle investigator, Assiut University) — Principal investigator
First posted
Mar 19, 2018
Start date
May 1, 2018
Primary completion
Nov 1, 2019 (estimated)
Completion
Feb 1, 2020 (estimated)
Last update
Jul 6, 2018

Study contacts

Mahmoud Mohamed Ragheb, Professor
Contact
Mmraghib@aun.edu.eg
00201003317723
Mohamed Hosam Eldeen Shokry, Fellow
Contact
hosam4hoss@yahoo.com
00201005685075

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jul 2018. You cannot join it, but the record below documents what was studied.

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