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Hearing Loss - ConductiveNCT02096809

Stability of the Cochlear Baha BI300/BA400 Implant System Loaded From 1 Week Post-surgery

A study testing One week loading of Bone Anchored Hearing Aid (BAHA) and Cochlear Baha BI300/BA400 Implant System in people with Hearing Loss - Conductive, run by Aarhus University Hospital at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Objectives To evaluate the safety of processor loading of the Cochlear BI300/BA400 implant system 1 week after implantation To evaluate the short term soft tissue healing and the long term skin reaction, with the new Cochlear BI300/BA400 implant system using the linear incision without subcutaneous tissue reduction. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Hearing Loss - Conductive
What is being tested?
One week loading of Bone Anchored Hearing Aid (BAHA) and Cochlear Baha BI300/BA400 Implant System
Could I receive a placebo?
No, everyone receives an active treatment
How many people
25 participants
Where
1 siteDenmark
Study dates
Mar 2014to Sep 2015
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients ≥ 18 years of age, with normal intelligence.
  • Absence of previous radiotherapy to the implant area.
  • Absence of active skin disease in the implant area.
  • Absence of diabetes.
  • Absence of osteoporosis
  • Absence of any relevant medical history or current disease/treatment/medication that may affect bone or skin quality in the implant area.

Who cannot join

  • No further

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Aarhus University Hospital, ENT-department

    Aarhus, 8000

Other trials in Denmark

About this study

Official title: Evaluation of Soft Tissue Healing and Implant Stability of Cochlear Baha BI300/BA400 Implant System Loaded From 1 Week Post-surgery After Linear Incision Without Soft Tissue Reduction.

Objectives

  • To evaluate the safety of processor loading of the Cochlear BI300/BA400 implant system 1 week after implantation
  • To evaluate the short term soft tissue healing and the long term skin reaction, with the new Cochlear BI300/BA400 implant system using the linear incision without subcutaneous tissue reduction.
  • To produce reference data regarding the stability of the BI300/BA400 implant system.
Read more

Study design: Prospective cohort study. Patients: 24 adults with anticipated normal skin and bone quality eligible for bone anchored implant surgery.

Intervention: Loading of the sound processor one week after surgery Main outcome measures: Implant stability, soft tissue reaction, skin overgrowth, pain and numbness will be assessed.

It is hypothesized that implant loading can be performed one week after surgery without any changes in implant stability, soft tissue reaction, skin overgrowth, pain or numbness around implant.

Read the detailed description

Background Implant stability

Until recently, the implants used in Baha surgery have exclusively been standard Brånemark type of titanium implants with an as-machined surface finish. The recommended procedure for Baha implantation with the machined titanium implants uses a 12-week healing period before loading the implant with a sound processor, in order to allow sufficient time for the implant to become integrated in the bone. The Cochlear Baha BI300 Series implant was designed to improve implant stability at placement and over time, thus making it possible to reduce the time to sound processor fitting. The implant features a wider diameter compared to the previous generation Baha implant, small-sized threads at the cylindrical portion of the implant underneath the flange, and a roughened implant surface due to formation of titanium oxide after blasting.

Six-month data from a multi-centre clinical investigation comparing the new implant with the previous generation Baha implant using a 6-week loading protocol, shows significantly higher Implant Stability Quotient (ISQ) values (measured by resonance frequency analysis) for the new implant at each time point, and no reduction in stability after loading (Dun et al., 2011). The data from the study suggest that the implant stability achieved 6 weeks after implantation is sufficient to support the sound processor. The data also suggest that a further reduction of the time to sound processor fitting may be possible, provided favourable bone conditions at the implant site and provided satisfactory soft tissue status at the time of loading. Hence, a clinical investigation with implant loading 21 days post-surgery was initiated by the team in Nijmegen, and 6-month data from the investigation confirm that it is safe to attach the sound processor after 3 weeks (Faber et al., 2012). Early results from two other studies using loading times of 4 weeks (McLarnon et al., 2012) and 2 weeks (Green et al., 2011), respectively, have also been presented and show good outcomes. All studies have been performed on patients with good bone quality.

Data from a prospective study with 49 patients loaded from 2 weeks post-surgery show no initial dip in stability and show no decrease in stability in the period after processor loading (ongoing study, awaiting publication). The stability of the implant in this study after one week is sufficient for processor loading at this time. No studies exist that investigates the effect on stability after processor loading 1 week postoperatively.

Implant stability measurement

The method of choice for implant stability measurements uses resonance frequency analysis (RFA) of a small magnetic rod attached to the abutment at the time of measuring (Osstell A/B, Gothenburg, Sweden). However, this method returns a number (Implant Stability Quotient, ISQ) for the stability that is dependent on the length of the abutment attached to the implant. To our knowledge there exists no clinical data that correlates the stability measurements made with different abutment length.

Soft tissue management

For three decades, the recommended procedure for Baha implantation advocated a hair free transplant measuring 25 x 25 mm placed direct on the periosteum. The purpose is to obtain an immobile skin, hence reducing the risk of adverse skin reactions in the area. Since there is no or only weak adherence between the abutment and surrounding soft tissue it is anticipated that, if no skin reduction is performed, epidermal down growth and pocket formation may occur over time, increasing the risk for infection in the implant area. This surgical procedure, with skin transplant, has proven safe; however, skin complications still occur and account for the majority of reported complications with Baha implants.

The newly introduced Cochlear BA400 abutment is covered with hydroxyapatite at the area of the abutment touching the skin and subcutaneous tissues. The abutment has been approved for surgery using a less invasive surgical technique (linear incision without subcutaneous tissue reduction) (www.cochlear.com). It has been shown in animal studies that the hydroxyapatite coating favours soft tissue healing without pocket formation (Larsson et al, 2012).

To our knowledge there exists no studies that compare the results with the BA400 inserted using the linear incision without subcutaneous tissue reduction with other abutments using the same technique.

Objectives

  • To evaluate the safety of processor loading of the Cochlear BI300/BA400 implant system 1 week after implantation
  • To evaluate the short term soft tissue healing and the long term skin reaction, with the new Cochlear BI300/BA400 implant system using the linear incision without subcutaneous tissue reduction.
  • To produce reference data regarding the stability of the BI300/BA400 implant system.

IMPLANT DEVICE

The following Conformité Européenne (CE) marked implant with pre-mounted abutment will be used (MDD Class IIb medical devices, manufacturer: Cochlear Bone Anchored Solutions, Mölnlycke, Sweden):

  • Cochlear Baha BI300 4 mm with Cochlear BA400 Abutment (DermalockTM). Length of the abutment will be decided after measuring the thickness of the skin with a specific tool.

TREATMENT

Surgery The implants will be placed according to the procedure for one-stage surgery. The surgical procedure is by a linear incision without removal of subcutaneous tissue. The implant will be places outside the linear incision. Only in cases where the longest available abutment (12mm) is deemed too short there will be performed a minimal soft tissue reduction of subcutaneous fatty tissue. A 5 mm punch will be used to punch the hole for the abutment in the skin flap.

All patients will receive treatment, thus no placebo control group is used. The surgical technique is the one recommended by the manufacturer for this type of implant and hence the study does not introduce any new surgical techniques or modifications hereof.

The risks with this treatment are: bleeding per- and postoperatively, wound infection and damage to surrounding tissues including sensory nerves to the scalp and loss of the implant. These risks are well known risks with known treatments and the study introduces no new risks.

Sound processor loading Sound processor fitting and loading will be performed 1 week after implant surgery, or at the discretion of the investigator. The decision to load an implant will be based on assessment of implant stability and status of the soft tissue. Patients who are evaluated as not ready to be loaded 1 week after surgery will be loaded as soon as the healing is sufficient.

ETHICAL CONSIDERATIONS There are no known extra risks or adverse effects of the new abutment compared to the previous abutment supplied by the manufacturer of the implant. Preliminary results (7) have shown promising positive effects on the soft tissue healing and implant stability. In conclusion, the new abutment design have the same potential adverse effects. All patients are offered the new abutment system.

The surgical technique: linear incision without soft tissue reduction, is recommended by the manufacturer to use with this implant system.

Stability measurements with radio frequency analysis have no known side effects.

The stability of the implant at the planned loading time (1 week) has been shown in previous studies to be better than that at which earlier generation implants has been loaded after 6 weeks(Dun et al., 2011,8). However, loading of the implant 1 week post-surgery has the potential risk of influencing the osseous integration of the implant in the cranial bone which could lead to loosening of the implant and eventually loss of implant. The patients will be controlled with stability measurement 1 week after loading of the implant and a possible loosening of the implant can be taken care of.

Loading of the implant 1 week post-surgery has potential benefits for the patient in the form of faster audiological rehabilitation and fewer visits to the hospital.

No specific recruitment of patients is made in this study. Patients referred to the hospital for Baha-surgery are evaluated according to the inclusion criteria and all patients (within the inclusion period) that are included are offered to be part of the study group.

Patients will be invited with a letter to a clinical examination prior to the operation. In this letter all patients are requested to bring an assessor if deemed necessary.

If the patient meets the inclusion criteria, spoken and written information about the study will be given by one of the investigators at the out-patient clinic. The examination and information will take place in a state-of-the-art examination room with no interruptions and there will be given time to discuss all relevant details of the study and questions will be answered.

The informed consent should be signed before the day of surgery. There will be approximately three weeks between the written information and the expected informed consent and questions can be answered in this period by contacting the investigators by e-mail or phone. If the patient decides not to participate in the study he will still be offered the operation with the same procedure, but the loading time will follow standard recommendations and no extra stability measurements will be performed.

SAMPLE SIZE CALCULATION To detect a difference in ISQ between baseline and any measurement point during follow up of 4 ISQ points, the study needs 21 patients in each group, not accounting for drop-out (comparison of two means, st.d.=4 in each group (5), α=0,05 two-sided, power=90%). To allow for a drop-out rate of around 10%, we include 25 patients. The time estimated to include this number of patients is 3 months.

With 25 patients we will be able to detect a risk difference of 0,41 for having Holgers' index 0 or 1-4 in the two groups (comparison of two proportions, α=0,05 two-sided, power=90%).

STATISTICS

Results will be analysed on the basis of both descriptive and inferential statistics.

The following results will be reported

  • Baseline characteristics
  • Implant stability by visit, represented as a Line plot of Mean ISQ (95% confidence interval).
  • Difference of the mean ISQ between intervention and control group at each measurement point (students t-test).
  • Average implant stability, as assessed by the mean area under the curve of ISQ-measurements (mean, confidence interval).
  • Effect of implant loading on implant stability, as assessed by change in Mean ISQ from time of loading to subsequent visit(s) (paired t-tests, confidence interval).
  • Soft tissue reactions (Holgers' Index) at each measurement point (Mantel-Haenszel statistics)
  • Soft tissue overgrowth at each measurement point (Mantel-Haenszel statistics)
  • Presence of pain at each measurement point (Mantel-Haenszel statistics).
  • Presence of numbness at each measurement point (Mantel-Haenszel statistics).
  • Dichotomization of the Holgers' scale will be performed by categorizing Holgers' grade 0 and 1 as "No clinically significant tissue reaction" and Holgers' grade 2-5 as "Clinically significant tissue reaction" and comparisons made between groups with the Fischer exact test.
  • Implant loss, as assessed by survival analysis (if any).
Being tested
One week loading of Bone Anchored Hearing Aid (BAHA), Cochlear Baha BI300/BA400 Implant System
Keywords
Bone Conduction, Hearing loss - conductive, Osseointegration, Prostheses and Implants
Medical subject headings
Hearing Loss, Conductive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • One week loading of Bone Anchored Hearing Aid (BAHA)Procedure or surgery

    Patients in this arm will be fitted with the BAHA one week after surgery.

  • Cochlear Baha BI300/BA400 Implant SystemDevice

Study groups in NCT02096809
Study groupRoleWhat they receive
One week loading of Bone Anchored Hearing Aid (BAHA)ExperimentalBone Anchored Hearing Aid (BAHA) loading after one week
Receives: Procedure: One week loading of Bone Anchored Hearing Aid (BAHA); Device: Cochlear Baha BI300/BA400 Implant System

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Implant stability

    Implant stability quotient measured at day of surgery. Implant stability is assessed using resonance frequency analysis. The measurement renders Implant Stability Quotient (ISQ) values from 1 to 100. Two perpendicular measurements are performed at each implant. The highest and lowest ISQ value out of three measurements obtained at each time point will be recorded. Measurements will be performed at the abutment level, and the Osstell ISQ instrument and SmartPeg Type 55 (Osstell, Gothenburg, Sweden) will be used.

    Measured: Day of surgery

  2. Implant stability

    See description for Implant stability, day of surgery Implant stability is assessed using resonance frequency analysis.

    Measured: One week

  3. Implant stability

    See description for Implant stability, day of surgery Implant stability is assessed using resonance frequency analysis.

    Measured: Two weeks

  4. Implant stability

    See description for Implant stability, day of surgery Implant stability is assessed using resonance frequency analysis.

    Measured: One month

  5. Implant stability

    See description for Implant stability, day of surgery Implant stability is assessed using resonance frequency analysis.

    Measured: 3 months

  6. Implant stability

    See description for Implant stability, day of surgery Implant stability is assessed using resonance frequency analysis.

    Measured: 6 months

  7. Implant stability

    See description for Implant stability, day of surgery Implant stability is assessed using resonance frequency analysis.

    Measured: 12 months

Secondary outcomes (24)
  1. Soft tissue status

    1. No irritation: epithelial debris removed if present.
    2. Slight redness: temporary local treatment indicated.
    3. Red and slightly moist; no granulation tissue present.
    4. Red and moist with granulation tissue, skin overgrowth, or scar formation: Local treatment indicated.
    5. Extensive granulation, skin overgrowth, or scar formation requiring revision surgery.
    6. Removal of skin-penetrating abutment necessary to control infection.

    Measured: One week

  2. Soft tissue status

    See description for soft tissue status, one week.

    1. No irritation: epithelial debris removed if present.
    2. Slight redness: temporary local treatment indicated.
    3. Red and slightly moist; no granulation tissue present.
    4. Red and moist with granulation tissue, skin overgrowth, or scar formation: Local treatment indicated.
    5. Extensive granulation, skin overgrowth, or scar formation requiring revision surgery.
    6. Removal of skin-penetrating abutment necessary to control infection.

    Measured: Two weeks

  3. Soft tissue status

    See description for soft tissue status, one week.

    1. No irritation: epithelial debris removed if present.
    2. Slight redness: temporary local treatment indicated.
    3. Red and slightly moist; no granulation tissue present.
    4. Red and moist with granulation tissue, skin overgrowth, or scar formation: Local treatment indicated.
    5. Extensive granulation, skin overgrowth, or scar formation requiring revision surgery.
    6. Removal of skin-penetrating abutment necessary to control infection.

    Measured: One month

  4. Soft tissue status

    See description for soft tissue status, one week.

    1. No irritation: epithelial debris removed if present.
    2. Slight redness: temporary local treatment indicated.
    3. Red and slightly moist; no granulation tissue present.
    4. Red and moist with granulation tissue, skin overgrowth, or scar formation: Local treatment indicated.
    5. Extensive granulation, skin overgrowth, or scar formation requiring revision surgery.
    6. Removal of skin-penetrating abutment necessary to control infection.

    Measured: 3 months

  5. Soft tissue status

    See description for soft tissue status, one week.

    1. No irritation: epithelial debris removed if present.
    2. Slight redness: temporary local treatment indicated.
    3. Red and slightly moist; no granulation tissue present.
    4. Red and moist with granulation tissue, skin overgrowth, or scar formation: Local treatment indicated.
    5. Extensive granulation, skin overgrowth, or scar formation requiring revision surgery.
    6. Removal of skin-penetrating abutment necessary to control infection.

    Measured: 6 months

  6. Soft tissue status

    See description for soft tissue status, one week.

    1. No irritation: epithelial debris removed if present.
    2. Slight redness: temporary local treatment indicated.
    3. Red and slightly moist; no granulation tissue present.
    4. Red and moist with granulation tissue, skin overgrowth, or scar formation: Local treatment indicated.
    5. Extensive granulation, skin overgrowth, or scar formation requiring revision surgery.
    6. Removal of skin-penetrating abutment necessary to control infection.

    Measured: 12 months

  7. Skin overgrowth

    1. No soft tissue thickening or overgrowth,
    2. Slight soft tissue thickening or overgrowth,
    3. Moderate soft tissue thickening or overgrowth. Local treatment and extra controls as indicated,
    4. Marked/distinct soft tissue thickening or overgrowth. Revision surgery is indicated.

    Measured: One week

  8. Skin overgrowth

    See description for skin overgrowth, one week. 0. No soft tissue thickening or overgrowth,

    1. Slight soft tissue thickening or overgrowth,
    2. Moderate soft tissue thickening or overgrowth. Local treatment and extra controls as indicated,
    3. Marked/distinct soft tissue thickening or overgrowth. Revision surgery is indicated.

    Measured: Two weeks

  9. Skin overgrowth

    See description for skin overgrowth, one week. 0. No soft tissue thickening or overgrowth,

    1. Slight soft tissue thickening or overgrowth,
    2. Moderate soft tissue thickening or overgrowth. Local treatment and extra controls as indicated,
    3. Marked/distinct soft tissue thickening or overgrowth. Revision surgery is indicated.

    Measured: One month

  10. Skin overgrowth

    See description for skin overgrowth, one week. 0. No soft tissue thickening or overgrowth,

    1. Slight soft tissue thickening or overgrowth,
    2. Moderate soft tissue thickening or overgrowth. Local treatment and extra controls as indicated,
    3. Marked/distinct soft tissue thickening or overgrowth. Revision surgery is indicated.

    Measured: 3 months

  11. Skin overgrowth

    See description for skin overgrowth, one week. 0. No soft tissue thickening or overgrowth,

    1. Slight soft tissue thickening or overgrowth,
    2. Moderate soft tissue thickening or overgrowth. Local treatment and extra controls as indicated,
    3. Marked/distinct soft tissue thickening or overgrowth. Revision surgery is indicated.

    Measured: 6 months

  12. Skin overgrowth

    See description for skin overgrowth, one week. 0. No soft tissue thickening or overgrowth,

    1. Slight soft tissue thickening or overgrowth,
    2. Moderate soft tissue thickening or overgrowth. Local treatment and extra controls as indicated,
    3. Marked/distinct soft tissue thickening or overgrowth. Revision surgery is indicated.

    Measured: 12 months

  13. Pain around implant

    Pain will be assessed using categories based on a VAS from 0-10:

    • None 0
    • Mild 1-3
    • Moderate 4-6
    • Extensive 7-10

    Measured: One week

  14. Pain around implant

    See description for pain around implant, one week

    None 0 Mild 1-3 Moderate 4-6 Extensive 7-10

    Measured: Two weeks

  15. Pain around implant

    See description for pain around implant, one week

    None 0 Mild 1-3 Moderate 4-6 Extensive 7-10

    Measured: One month

  16. Pain around implant

    See description for pain around implant, one week

    None 0 Mild 1-3 Moderate 4-6 Extensive 7-10

    Measured: 3 months

  17. Pain around implant

    See description for pain around implant, one week

    None 0 Mild 1-3 Moderate 4-6 Extensive 7-10

    Measured: 6 months

  18. Pain around implant

    See description for pain around implant, one week

    None 0 Mild 1-3 Moderate 4-6 Extensive 7-10

    Measured: 12 months

  19. Numbness around implant

    Numbness will be assessed using categories based on a measurement of the largest distance from the abutment with altered or no sensitivity:

    • None ≤ 1cm
    • Mild 1 - 3cm
    • Moderate 3 - 5 cm
    • Extensive ≥ 5cm

    Measured: One week

  20. Numbness around implant

    See description fot numbness around implant, one week

    None ≤ 1cm Mild 1 - 3cm Moderate 3 - 5 cm Extensive ≥ 5cm

    Measured: Two weeks

  21. Numbness around implant

    See description fot numbness around implant, one week

    None ≤ 1cm Mild 1 - 3cm Moderate 3 - 5 cm Extensive ≥ 5cm

    Measured: One month

  22. Numbness around implant

    See description fot numbness around implant, one week

    None ≤ 1cm Mild 1 - 3cm Moderate 3 - 5 cm Extensive ≥ 5cm

    Measured: 3 months

  23. Numbness around implant

    See description fot numbness around implant, one week

    None ≤ 1cm Mild 1 - 3cm Moderate 3 - 5 cm Extensive ≥ 5cm

    Measured: 6 months

  24. Numbness around implant

    See description fot numbness around implant, one week

    None ≤ 1cm Mild 1 - 3cm Moderate 3 - 5 cm Extensive ≥ 5cm

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Mar 2014 (estimated)
  2. Study startMar 2014
  3. Primary completionAug 2014
  4. Study completionSep 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
25 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02096809
Sponsor's protocol ID
1-10-72-5-14
Other IDs
1-10-72-5-14
Status last verified
Dec 2015
First submitted
23 Mar 2014
Last updated
8 Dec 2015
Results posted
No
Data monitoring committee
No

Publications

  • Dun CA, de Wolf MJ, Hol MK, Wigren S, Eeg-Olofsson M, Green K, Karlsmo A, Flynn MC, Stalfors J, Rothera M, Mylanus EA, Cremers CW. Stability, survival, and tolerability of a novel baha implant system: six-month data from a multicenter clinical investigation. Otol Neurotol. 2011 Aug;32(6):1001-7. doi: 10.1097/MAO.0b013e3182267e9c.

    PubMed 21725257
  • Larsson A, Wigren S, Andersson M, Ekeroth G, Flynn M, Nannmark U. Histologic evaluation of soft tissue integration of experimental abutments for bone anchored hearing implants using surgery without soft tissue reduction. Otol Neurotol. 2012 Oct;33(8):1445-51. doi: 10.1097/MAO.0b013e318268d4e0.

    PubMed 22918110
  • Faber HT, Dun CA, Nelissen RC, Mylanus EA, Cremers CW, Hol MK. Bone-anchored hearing implant loading at 3 weeks: stability and tolerability after 6 months. Otol Neurotol. 2013 Jan;34(1):104-10. doi: 10.1097/MAO.0b013e318277a282.

    PubMed 23202148
  • Holgers KM, Tjellstrom A, Bjursten LM, Erlandsson BE. Soft tissue reactions around percutaneous implants: a clinical study of soft tissue conditions around skin-penetrating titanium implants for bone-anchored hearing aids. Am J Otol. 1988 Jan;9(1):56-9.

    PubMed 3364537
  • Wazen JJ, Young DL, Farrugia MC, Chandrasekhar SS, Ghossaini SN, Borik J, Soneru C, Spitzer JB. Successes and complications of the Baha system. Otol Neurotol. 2008 Dec;29(8):1115-9. doi: 10.1097/MAO.0b013e318187e186.

    PubMed 18833013
  • McLarnon CM, Johnson I, Davison T, Hill J, Henderson B, Leese D, Marley S. Evidence for early loading of osseointegrated implants for bone conduction at 4 weeks. Otol Neurotol. 2012 Dec;33(9):1578-82. doi: 10.1097/MAO.0b013e31826dba5f.

    PubMed 23069746

Questions about this trial

What is this clinical trial studying?

A study testing One week loading of Bone Anchored Hearing Aid (BAHA) and Cochlear Baha BI300/BA400 Implant System in people with Hearing Loss - Conductive, run by Aarhus University Hospital at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Dec 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Implant stability (time frame: Day of surgery). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02096809, which also lists 6 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Dec 2015.

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