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Clinical Trials/NCT04611698
NCT04611698
Completed
N/A

Immediate Loading of Bone Anchored Hearing Devices

Manchester University NHS Foundation Trust0 sites1 target enrollmentJune 2016
ConditionsHearing Loss

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hearing Loss
Sponsor
Manchester University NHS Foundation Trust
Enrollment
1
Primary Endpoint
Compare device stability and rate of successful implantation
Status
Completed
Last Updated
3 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
December 31, 2017
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Compare device stability and rate of successful implantation

Time Frame: 12 months

Measuring 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 Outcomes

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

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