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Recruiting Not applicable

Intracochlear Platelet-rich Fibrin Application in Cochlear Implantation

NCT05215197 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2022-01-31
Last updated
2026-07-14

Condition(s) studied

Hearing Loss, Sensorineural

Investigational drug(s) / intervention(s)

intracochlear platelet rich fibrin administration

intracochlear platelet rich fibrin administration: intracochlear platelet rich fibrin administration during routine cochlear implantation surgery

Study summary

Fibrosis due to surgical trauma is a common problem with cochlear implants. Fibrosis limits the effectiveness of implant and increases the power consumption. Our aim in this study is to benefit from the anti-inflammatory effects of autologous platelet-rich fibrin to reducing the fibrotic cascade.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with sensorineural hearing loss * Patients who will have cochlear implant surgery with CI422 electrode Exclusion Criteria: * Patients with cochlear abnormality * Patients with auditory neuropathy

Primary outcome measure(s)

  • Electrode Impedance(Ohm) — 1-6 months
    All intra-operative impedance values will be acquired after surgery. They will be repeated in first week, 1, 3 and 6th months

Trial sites (1)

FacilityCityRegionStatus
Pamukkale University Denizli Turkey (Türkiye) Recruiting
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 NCT05215197 on ClinicalTrials.gov ↗ ← All trials in Turkey