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NCT05494632 · ClinicalTrials.gov registry record · NA

Interaural Frequency and Loudness Mismatch in SSD CI Users

A NA study of Outcomes, sponsored by Washington University School of Medicine.

Completed
Registry status
NA
Development phase
45
Enrollment target
1
Study location

NCT05494632 is a NA study of Outcomes that has completed, run by Washington University School of Medicine. The registered enrollment target is 45 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT05494632, a NA study of Outcomes, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
NA
Development phase
45 participants
Enrollment target
1
Study location

Study Summary

Interaural loudness and pitch mismatch in single-sided deaf cochlear implant (SSD-CI) recipients reduces binaural processing cues and contributes to performance outcomes, specifically speech understanding in noise and localization. The study aims to improve binaural cues through speech processor program modifications that reduce interaural mismatches.

Conditions Studied

Interventions

  • DEVICE Treatment-modifications to CI speech processor program. Specifically reducing interaural frequency mismatch in experienced SSD-CI recipients.
  • DEVICE Treatment-modifications to CI speech processor program to reduced interaural frequency mismatch in newly implanted SSD-CI recipients.
  • DEVICE Treatment-modifications to CI speech processor program to reduced interaural loudness mismatch in experienced SSD-CI recipients.

Study Locations (1)

Missouri

  • Washington University School of Medicine - St Louis

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2022-08-12
Est. Completion 2025-08-01
Phase NA

What the Registry Record Tells You About NCT05494632

The ClinicalTrials.gov registry entry for NCT05494632 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Outcomes appearing as the primary indexed condition, and to 3 interventions - of which Treatment-modifications to CI speech processor program. Specifically reducing interaural frequency mismatch in experienced SSD-CI recipients. is the first listed.

NCT05494632 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT05494632 about?

NCT05494632 is a clinical study titled "Interaural Frequency and Loudness Mismatch in SSD CI Users". Interaural loudness and pitch mismatch in single-sided deaf cochlear implant (SSD-CI) recipients reduces binaural processing cues and contributes to performance outcomes, specifically speech understanding in noise and localization. The study aims to improve binaural cues through speech processor pro...

What is the current status of trial NCT05494632?

This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2022-08-12. Estimated completion is 2025-08-01.

What conditions does trial NCT05494632 study?

This clinical trial studies the following conditions: Outcomes.

What interventions are being tested in trial NCT05494632?

The interventions under investigation include: Treatment-modifications to CI speech processor program. Specifically reducing interaural frequency mismatch in experienced SSD-CI recipients. (DEVICE), Treatment-modifications to CI speech processor program to reduced interaural frequency mismatch in newly implanted SSD-CI recipients. (DEVICE), Treatment-modifications to CI speech processor program to reduced interaural loudness mismatch in experienced SSD-CI recipients. (DEVICE).

Who is sponsoring clinical trial NCT05494632?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05494632 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.