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Cross-sectional and Prospective Study to Characterize Early-onset Presbycusis
NCT06354010 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to characterize and assess the evolution of hearing impairment of patients with adulthood-onset bilateral sensorineural hearing loss carrying mutations on GJB2 gene.
Conditions Studied
Interventions
- GENETIC Genotyping
- OTHER Audiological assessments
Study Locations (2)
Florida
- The University of South Florida Board of Trustees — Tampa
Other
- CHU Gui de Chauliac — Montpellier
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-06-14 |
| Est. Completion | 2027-07 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06354010
The ClinicalTrials.gov registry entry for NCT06354010 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Sensorion, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Sensorineural Hearing Loss, Bilateral appearing as the primary indexed condition, and to 2 interventions — of which Genotyping is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06354010 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Florida, Other. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06354010 about?
NCT06354010 is a clinical study titled "Cross-sectional and Prospective Study to Characterize Early-onset Presbycusis". The purpose of this study is to characterize and assess the evolution of hearing impairment of patients with adulthood-onset bilateral sensorineural hearing loss carrying mutations on GJB2 gene.
What is the current status of trial NCT06354010?
This trial is currently recruiting. The enrollment target is 100 participants. The study started on 2024-06-14. Estimated completion is 2027-07.
What conditions does trial NCT06354010 study?
This clinical trial studies the following conditions: Sensorineural Hearing Loss, Bilateral. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06354010?
The interventions under investigation include: Genotyping (GENETIC), Audiological assessments (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06354010?
This trial is sponsored by Sensorion, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06354010 being conducted?
This trial has 2 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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