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NCT06106373 · ClinicalTrials.gov registry record · NA
iotaSOFT Pediatric Study
A NA study, sponsored by iotaMotion.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT06106373: Completed NA study, sponsored by iotaMotion.
NCT06106373 is a NA study that has completed, run by iotaMotion. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06106373, a NA study, has completed, sponsored by iotaMotion.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
Prospective, non-randomized, open-label study to evaluate the safety and efficacy of the iotaSOFT Insertion System when used to assist electrode array insertion during cochlear implant surgery in a pediatric population.
Primary Outcome
The primary endpoint of the study was to demonstrate safety of the iotaSOFT Insertion System through evaluation of iotaSOFT related serious adverse events through 30 days after CI surgery/activation.
Interventions
- DEVICE iotaSOFT Insertion System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2022-05-17 |
| Est. Completion | 2025-07-10 |
| Phase | NA |
What the finished NCT06106373 record still lists
NCT06106373 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which iotaSOFT Insertion System is the first listed.
NCT06106373 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06106373 about?
NCT06106373 is a clinical study titled "iotaSOFT Pediatric Study". Prospective, non-randomized, open-label study to evaluate the safety and efficacy of the iotaSOFT Insertion System when used to assist electrode array insertion during cochlear implant surgery in a pediatric population.
What is the current status of trial NCT06106373?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2022-05-17. Estimated completion is 2025-07-10.
What interventions are being tested in trial NCT06106373?
The interventions under investigation include: iotaSOFT Insertion System (DEVICE).
Who is sponsoring clinical trial NCT06106373?
This trial is sponsored by iotaMotion, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06106373's enrollment target sits among peer trials
20 1768th of 2000 higher than 140 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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