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Standard Post Market Clinical Follow-up (PMCF) Study WSA 2026

NCT07667140 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2026-06-24

No results posted yet for this study

Summary

The purpose of the study is to follow-up on a released low-risk device as part of standard PMCF activities.

Conditions

  • Hearing Loss, Sensorineural

Interventions

DEVICE

In-the-Ear Hearing Aid

Custom In-the-Ear hearing aid. Form Factor In the Canal (ITC)

DEVICE

Own hearing aid

subjects' own hearing aids, any brand, any model

DEVICE

In-the-Ear Hearing Aid

Instant Fit Hearing Aid, Form Factor CIC

Sponsors & Collaborators

  • Hoerzentrum Oldenburg

    collaborator UNKNOWN

  • WSAUD A/S

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-25
Primary Completion
2026-04-30
Completion
2026-04-30

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07667140 on ClinicalTrials.gov