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Clinical Trials in Germany / NCT06841900
Starting soon Observational

Implementation of the International Classification of Functioning, Disability and Health Model in Paediatric Cochlear Implant Recipients

NCT06841900 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2025-03
Last updated
2025-02-28

Condition(s) studied

Cochlear Impant Children

Investigational drug(s) / intervention(s)

Cochlear Implantation

Cochlear Implantation: Standard cochlear implantation

Study summary

The aim of this study is to implement the International Classification of Functioning, disability and health (ICF) in paediatric Cochlear Implant (CI) recipients (\<18 years) with prelingual sensorineural hearing loss in a multicenter prospective study to evaluate audiological rehabilitation after cochlear implantation. For this, ICF qualifiers which denote the magnitude of the level of health or severity of the problem will be quantified. Outcome measures include four questionnaires and three standard audiological examinations. Subjects will be assessed up to 1 month before implantation and 3 months, 6 months and 1 year post the activation of the speech processor.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: General * Children aged \< 18 years with prelingual bilateral severe-to-profound HL * Signed and dated informed consent, informed permission and/or minor's assent. * Willingness to participate in evaluations, test sessions, and medical follow-up sessions as defined in the protocol. * Physical and mental competence to participate in fitting of the device and follow-up sessions as defined in the protocol. Audiological * Completion of hearing assessment battery showing suitability of the CI candidates. * Compliance with cochlear implant candidate selection criteria of the implanting centre. * First cochlear implantation Medical * Patent cochlea, as evidenced by High-resolution computed tomography (HRCT) and/or Magnetic Resonance Imaging (MRI). Exclusion Criteria: General * Re-implantation of the cochlear implant * No motivation to participate in the study and/or unreasonable expectations. Medical * Presence of contra-indications for surgery in general and cochlear implantation in particular. * Presence of central auditory lesions. * Any disorder that may relate to an increased risk of skin flap problems Use of one of the following electrodes for implantation * Compressed * Split * Any type of custom made electrodes

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
Fiona Stanley Fremantle Hospital Group Perth Australia
University Hospital Antwerp Edegem Belgium
University Clinic of Würzburg Würzburg Germany
World Hearing Centre Warsaw Poland
King Abdullah Ear Specialist Center (KAESC) Riyadh Saudi Arabia
Hospital La Paz Madrid Spain

More University Hospital, Antwerp trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06841900 on ClinicalTrials.gov ↗ ← All trials in Germany