Cochlear Implantation Experience
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: cochlear implantation.
- Who it may be relevant to
- Registry conditions: Cochlear Function Disorder. Basic parameters: 1 year — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Cochlear Implantation in Assiut University Hospital Experience
Overview
Evaluating the effectiveness and outcomes of cochlear implants in individuals with hearing loss,identifying common complications or risks associated with cochlear implantation, including device failure, surgical complications, or issues related to the patient's anatomy
Interventions
- Procedure cochlear implantation
After the surgery, patients typically undergo a period of recovery and healing. several factors including age at implantation, pre- and post-operative therapy, and parental involvement
Primary outcome measures
- Post-Surgical Complication Rate: Infection, device failure,Measures auditory progression [Time frame: Baseline]
Eligibility criteria
Inclusion criteria
- Patients with severe to profound bilateral sensorineural hearing loss who were candidates for CI.
Patients who regularly use their cochlear implant device as recommended.
Exclusion criteria
- Non-Sensorineural Hearing Loss - Non-Functional Auditory Nerve - . Severe Mental or Cognitive Impairments
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-control
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06896864 · CI experience