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Immediate Loading of Bone Anchored Hearing Devices

Immediate Loading of Bone Anchored Hearing Devices

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04611698
Enrollment
1
Registered
2020-11-02
Start date
2016-06-30
Completion date
2017-12-31
Last updated
2023-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Loss

Brief summary

Bone anchored hearing aids provide a hearing solution for patients that are unable to wear traditional air conduction hearing aid solutions. The technology of the devices has developed significantly over the last 510 years and patients are gaining access to their sound processor at a much earlier stage than when first brought onto the market. Despite this the investigators feel there is still room to develop this and with the new abutments with specialised hydroxyapatite coating it is hoped that patients can be loaded with their sound processor in the day of surgery. This study will compare abutment stability between two groups of patients. Those loaded immediately with their sound processor and those loaded traditionally at 2 weeks post operatively. At routine followup appointments patients will have the stability of their abutment checked and the investigators will compare to see if loading earlier had any detrimental effects on osteointegration and the stability of the abutment. Based on the favourable outcomes and high stability record for the BA400 it is anticipated that the time to processor fitting may be further reduced, provided favourable bone conditions at the implant site and provided satisfactory soft tissue status at the time of loading. It is hypothesised that loading immediately at the time of surgery is possible with comparable short and long term outcomes when compared to standard loading at 2 weeks

Interventions

DEVICEBaha sound processor BA400

Baha sound processor BA400 is a cochlear implant designed specifically for soft tissue preservation.

Sponsors

Northern Care Alliance NHS Foundation Trust
CollaboratorOTHER
Manchester University NHS Foundation Trust
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* Patients eligible for receiving the Baha system.

Exclusion criteria

* Adult patients, i.e. ≥18 years * Eligible for the Baha system * Bone thickness at the implant site of at least 4 mm * No known disease or treatment that compromises / will compromise the bone quality at the implant site

Design outcomes

Primary

MeasureTime frameDescription
Compare device stability and rate of successful implantation12 monthsMeasuring device stability and rate of successful implantation for patients fitted with the Baha BA400 immediately on the day of surgery and at fitting 2 weeks post operatively. A successful implant is an implant that osseointegrates and is stable over time when supporting the load of the Baha sound processor.

Secondary

MeasureTime frame
Measure the stability, as determined by Implant Stability Quotient (ISQ) values, of Baha implants placed immediately and at 23 weeks post operatively.23 weeks
Record implant survival over time.12 months
Monitor the status of the periimplant soft tissue using the classification proposed by Holgers' et al.12 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026