Partial EdentulismLunaNCT01529801
Assessment of the Effect of a Novel Surface Roughness Treatment on Dental Implants on Integration Success
A study testing Osseotite Certain Tapered Group A, Osseotite Certain Tapered Group B and Osseotite Certain Tapered Group C in people with Partial Edentulism and Tooth Disease, run by ZimVie at 1 site in Chile.
Trial summary
A study where dental implants with different roughened surfaces will be evaluated for the ability to resist countertorque forces. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Partial Edentulism, Tooth Disease
- What is being tested?
- Osseotite Certain Tapered Group A, Osseotite Certain Tapered Group B and Osseotite Certain Tapered Group C
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteChile
- Study dates
- Feb 2011to Nov 2016
- 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 of either sex and older than 18 years of age
- patients needing at least one dental implant to treat partial edentulism
- patients physically able to tolerate surgical and restorative dental procedures
- patients agreeing to all protocol visits
Who cannot join
- patients with infection or severe inflammation at the intended treatment sites
- patients smoking greater than 10 cigarettes per day
- patients with uncontrolled diabetes mellitus
- patients with uncontrolled metabolic diseases
- patients who received radiation treatment to the head in the past 12 months
- patients needing bone grafting at the intended treatment sites
- patients known to be pregnant at screening visit
- patients with para-functional habits like bruxing and clenching
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Prospective Randomized-controlled Study of the Effect of Surface Topographies on Implant Integration Rates and Clinical Success
A study where dental implants with different roughened surfaces will be evaluated for the ability to resist countertorque forces.
Read the detailed description
This study on dental implants with different roughened surfaces will assess its ability to resist countertorque testing at various study time points and demonstrate high success
- Conditions
- Partial Edentulism, Tooth Disease
- Being tested
- Osseotite Certain Tapered Group A, Osseotite Certain Tapered Group B, Osseotite Certain Tapered Group C
- Keywords
- edentulism, dental implants, clinical study, randomized, Osseotite Certain Tapered, Crestal bone level
- Medical subject headings
- Tooth Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Osseotite Certain Tapered Group ADevice
Also called Osseotite endosseous dental implant
Osseotite Certain Tapered with different surface roughness
Osseotite Certain Tapered Group BDevice
Also called Osseotite endosseous dental implant
Osseotite Certain Tapered with different surface roughness
Osseotite Certain Tapered Group CDevice
Also called osseotite endosseous dental implant
Osseotite Certain Tapered with different surface roughness
| Study group | Role | What they receive |
|---|---|---|
| Roughness group A | Experimental | Osseotite Certain Tapered Group A Receives: Device: Osseotite Certain Tapered Group A |
| Roughness Group B | Experimental | Osseotite Certain Tapered Group B Receives: Device: Osseotite Certain Tapered Group B |
| Roughness Group C | Experimental | Osseotite Certain Tapered Group C Receives: Device: Osseotite Certain Tapered Group C |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary stability countertorque measures
Resistance to countertorque measures showing primary stability and success of the implant
Measured: 6 weeks
Secondary outcomes (1)
Cumulative success rate
Crestal bone regression (amount of bone loss measured) and equivalence in integration success (implant mobility)
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Feb 2012 (estimated)
- Study startFeb 2011
- Primary completionNov 2016
- Study completionNov 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Partial EdentulismStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- ZimVie
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Jaime Acuna, DDS, Principal investigator, Hospital San Jose
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01529801
- Sponsor's protocol ID
- 3011
- Acronym
- Luna
- Status last verified
- Mar 2022
- First submitted
- 7 Feb 2012
- Last updated
- 28 Mar 2022
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Mar 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective Randomized-controlled Study of the Effect of Surface Topographies on Implant Integration Rates and Clinical Success
- ClinicalTrials.gov ID
- NCT01529801
- Acronym / sponsor ID
- Luna / 3011
- Conditions
- Partial Edentulism, Tooth Disease
- Keywords
- edentulism, dental implants, clinical study, randomized, Osseotite Certain Tapered, Crestal bone level
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 80 participants (actual)
- Lead sponsor
- ZimVieIndustry (pharma, biotech, devices)
- Study start
- Feb 2011
- Primary completion
- Nov 2016 (actual)
- Study completion
- Nov 2016 (actual)
- First posted
- 9 Feb 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A study where dental implants with different roughened surfaces will be evaluated for the ability to resist countertorque forces.
Detailed description
This study on dental implants with different roughened surfaces will assess its ability to resist countertorque testing at various study time points and demonstrate high success
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Roughness group A | Experimental | Device: Osseotite Certain Tapered Group AOsseotite Certain Tapered Group A |
| Roughness Group B | Experimental | Device: Osseotite Certain Tapered Group BOsseotite Certain Tapered Group B |
| Roughness Group C | Experimental | Device: Osseotite Certain Tapered Group COsseotite Certain Tapered Group C |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- patients of either sex and older than 18 years of age
- patients needing at least one dental implant to treat partial edentulism
- patients physically able to tolerate surgical and restorative dental procedures
- patients agreeing to all protocol visits
Key exclusion criteria (8 listed)
- patients with infection or severe inflammation at the intended treatment sites
- patients smoking greater than 10 cigarettes per day
- patients with uncontrolled diabetes mellitus
- patients with uncontrolled metabolic diseases
- patients who received radiation treatment to the head in the past 12 months
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Osseotite Certain Tapered Group AAlso: Osseotite endosseous dental implantOsseotite Certain Tapered with different surface roughness | Device | Roughness group A |
| Osseotite Certain Tapered Group BAlso: Osseotite endosseous dental implantOsseotite Certain Tapered with different surface roughness | Device | Roughness Group B |
| Osseotite Certain Tapered Group CAlso: osseotite endosseous dental implantOsseotite Certain Tapered with different surface roughness | Device | Roughness Group C |
Primary outcome
Primary stability countertorque measures
Time frame: 6 weeks
Resistance to countertorque measures showing primary stability and success of the implant
1 secondary outcome
Cumulative success rate
Time frame: 2 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Mar 2022.
- Individual participant dataSharing planned: No
Related trials for Partial Edentulism
Not yet recruitingObservational study
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Comparative Evaluation of Artificial Intelligence-Assisted Versus Conventional Guided Implant Planning in Free End Saddle Cases
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Immediate vs Conventional Loading With Different Crown Materials on Immediately Placed Single Implants
Partial Edentulism, Dental Implant
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Clinical Fit of Conventionally Cast and 0° SLM Removable Partial Denture Frameworks
Partial Edentulism Class 3, Removable Partial Denture
Active, not recruitingObservational study
Survival of Implant-Supported All-Ceramic Prostheses
Partial Edentulism, Disorder of Prostheses and Implants
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jaime Acuna, DDS principal investigator
Hospital San Jose
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Osseotite Certain Tapered Group A, Osseotite Certain Tapered Group B and Osseotite Certain Tapered Group C in people with Partial Edentulism and Tooth Disease, run by ZimVie at 1 site in Chile.
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 4 inclusion and 8 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 28 Mar 2022. 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 Chile. 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?
Primary stability countertorque measures (time frame: 6 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 28 Mar 2022.