Dental Implant FailedNCT04432519
Multi-level Dimensional Changes at Immediate Implant Sites
A study testing Immediate dental implant placement in people with Dental Implant Failed, run by Universidade Católica Portuguesa at 1 site in Portugal.
Trial summary
Studies evaluating the use of customized healing screws/abutments in immediate implant placement have been performed, aiming to assess possible advantages with the use of this treatment modality. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Dental Implant Failed
- What is being tested?
- Immediate dental implant placement
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 28 participants
- Where
- 1 sitePortugal
- Study dates
- 1 Jun 2019to 8 Jun 2020
- 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
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- patients with ≥18 years of age;
- patients who had a failing tooth and needed an implant placing therapy in the aesthetic zone (between 15-25);
- the failing tooth has adjacent and opposing natural teeth;
- sufficient mesial-distal and inter-occlusal space for placement of the implant and definitive restoration;
- had an intact socket wall previously to the extraction;
- had sufficient apical bone to place an immediate implant with minimum primary stability of 30 N/cm.
Who cannot join
- individuals diagnosed with periodontal disease;
- medical and general contraindications for the surgical procedure;
- heavy smokers (> 10 cigarettes/day); .an active infection at the implant site.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Linear and Volumetric Analysis on the Effect of Customized Healing Abutments at Maxillary Immediate Implant Sites: a Prospective Randomized Clinical Trial
Studies evaluating the use of customized healing screws/abutments in immediate implant placement have been performed, aiming to assess possible advantages with the use of this treatment modality. Despite the existence of these investigations, there is a lack of information regarding a digital approach to evaluate in an objective manner soft and hard tissue dimensional changes at this treatment modality.
Read the detailed description
Studies evaluating the use of customized healing screws/abutments have been performed aiming to assess possible advantages with the use of this treatment modality. Despite the existence of these investigations, there is a lack of information regarding a digital approach to evaluate in an objective manner soft and hard tissue dimensional changes.
The aim of this study is to perform a volumetric analysis evaluating peri-implant tissues dimensional changes on the effect of using customized healing abutments compared with the use of collagen matrices as socket sealing options in maxillary immediate implant placement.
The present study was designed as a prospective, randomized, controlled clinical trial with a parallel-group design, to document the response of using a customized healing abutment in maxillary immediate implants. Twenty-eight consecutive patients in need of a single implant restoration in the maxillary arch following tooth extraction were included in this study.
All patients were treated with cylindrical shape implants (OsseoSpeed EV™, AstraTech Implant System, Dentsply Implants, Möhndal, Sweden) with a narrow diameter internal connection platform following the surgical sequence protocol provided by the manufacturer. The implant was placed in a correct three-dimensional position, engaging the palatal and apical bone to achieve high primary stability. (Buser et al. 2004) After implant insertion, a gap of at least 2 mm between the inner cortical buccal bone plate and the implant surface was filled with DBBM material (Symbios®, Dentsply Implants, Möhndal, Sweden).
The two groups differ in the type of socket sealing. Control group fresh sockets were sealed with a resorbable collagen membrane (Mucograf Seal®, Geistlish Biomaterials, Wolhusen, Switzerland) stabilised with single interrupted 6/0 polyamide sutures (SeralonTM, Serag-Wiessner, Nalia, Germany), whereas test group received a healing abutment customized with a composite resin material allowing to close the socket without sutures.
Clinical examination and image acquisition Examination protocol and data collection consisted of four appointments: 1) T0 (flapless tooth extraction and implant insertion; 2) T1 (1-month follow-up after implant placement; 3) T2 (4-month follow-up after implant insertion) and 4) T3 (1-year postoperative follow-up). An intraoral scan of the upper arch (Cerec Omnicam®, Sirona Dental Systems GmbH, Bensheim, Germany) and a CBCT radiographic evaluation (Ortophos XG 3D®, Sirona Dental Systems GmbH, Bensheim, Germany) were performed followed by tooth extraction and implant placement (T0). At this point, two clinical parameters were assessed with a periodontal probe to the nearest millimetre: BID (distance between implant shoulder and the buccal bone plate) and KM (distance between the gingival groove and the mucogingival junction). Intraoral scans were completed post-implant placement at one month (T1), four months (T2) and twelve months (T3). In all follow-up appointments hygiene instructions were given to the patients and a periodontal care was executed when necessary.
Matching digital models All digital models were exported from the intraoral scanner in STL format. The T0 and T1, T0 and T2, and T0 and T3 STL files were overlapped and a strict alignment was made into one common coordinate system. A final alignment was done through the best fit alignment algorithm for a perfect match of digital models and executed with settings adjusted to the oral cavity.
After the superimposition of digital models, a colour map was created to quantitatively analyse the three-dimensional changes occurring in the surgical areas and adjacent tissues. Green areas correspond to the perfect alignment of the model. The variation between yellow and red represents variations of volumetric increase, whereas the variations between light blue and dark blue represent the variations of volumetric decrease. A region of interest (ROI) with 10 section planes, perpendicular to the coronal section of the tooth, was computed at buccal and palatal aspect (Figure 2). These sections were set at the most apical point of the gingival margin and ended 5 mm above it. Mesially and distally, a line passing through the interproximal area limited the region of interest. The same ROI was used in each patient, at the different comparison points. The intersection of these sections with the overlapping models allowed the linear changes to be obtained in each area. The Mean Buccal Change (MBC0-1, MBC0-2, and MBC0-3) and Mean Total Change (MTC0-1, MTC0-2 and MTC0-3) were calculated in millimetres (mm) to evaluate the changes that occurred in peri-implant contour (Figure 3).
Digital models superimposed in Geomagic Control X® were exported to Materialise Magics® for volumetric assessment. A volumetric ROI was manually selected with "Cut or Punch" function using interproximal areas as mesial and distal limits. All cuts were performed in the same way in all digital models so that all measurements were carried out in the same areas. ROI volume at T0 was computed for further comparison with consecutive volume variation values (Figure 4). The 3D-analysis was conducted with "Boolean" functions, which allowed researchers to obtain the volume variation in each time point from different variables like the Buccal Volume Variation (BVv0-1, BVv0-2, and BVv0-3) and Total Volume Variation (TVv0-1, TVv0-2, e TVv0-3), computed in cubic millimetres (mm3). To allow a direct comparison of different sites at different time points, relative percentages of these variables were calculated based on the ROI volume at T0 (Szathvary et al. 2015). All measurements were recorded to the nearest 0.01 mm.
Radiographic assessment The acquisition of radiographic images was performed with a volumetric dimension of 8 x 8 cm for 14s with the tomography acquisition protocol, with a voxel size of 0.1 mm in HD mode. The CBCT images were imported in a DICOM format to Mimics® software to perform the measurements. Buccal plate thickness (BT) was assessed for 3D radiographic analysis to evaluate the initial features of the alveolar bone. All measurements were obtained through coronal slice reconstructions, using an adjacent line to the sinus/nasal plate as a reference (Figure 5). BT was measured 1 mm above the coronal bone margin using a central slice, as well at the mesial and distal slices, ranging 1 mm from the central slice. Mean BT values were obtained as the average values of the three slices. One independent examiner who was not involved in the study executed all measurements.
Statistical analysis The outcome variables were presented as mean values, standard deviation, median and 95% confidence interval. Measurement time (T1, T2 and T3) was considered as a factor and the following as covariates: age, gender, KM height, location, implant length, BID and BT. The statistical analysis was performed using SPSS™ Statistical Package for the Social Sciences, version 21.0 (IBM Corporation, Armonk, NY, USA). The Mann-Whitney U-test was used to disclose differences for continuous non-paired variables. Moreover, the paired Wilcoxon test was used when the normal distribution of the groups was proved. A multiple linear regression model, using the stepwise forward method, was built to analyse the effect of the tested treatment in the main outcome variables throughout the study. All hypothesis tests were conducted at the 5% level of significance.
- Conditions
- Dental Implant Failed
- Being tested
- Immediate dental implant placement
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Immediate dental implant placementProcedure or surgery
Also called Post extraction immediate implant placement
Dental implant insertion in the same surgical stage of the tooth extraction, consisting in implant placement in the fresh socket.
| Study group | Role | What they receive |
|---|---|---|
| Group CA | Experimental | Customized healing abutment inserted in immediate implant placement. Receives: Procedure: Immediate dental implant placement |
| Group CM | Active comparator | Resorbable Collagen Membrane for socket closure in immediate implant placement. Receives: Procedure: Immediate dental implant placement |
What is being measured
The primary outcome is the main question the study is designed to answer.
Buccal volume variation (BVv)
Variation of the alveolar volume at the buccal aspect. The 3D-analysis was conducted with "Boolean" functions, which allowed researchers to obtain the volume variation in each time point from different variables like the Buccal Volume Variation (BVv0-1, BVv0-2, and BVv0-3), computed in cubic millimetres (mm3) and To allow a direct comparison of different sites at different time points, relative percentages of these variables were calculated based on the ROI volume at T0.
Measured: Baseline (T0); 1 month (T1); 4 months (T2) and 12 months (T3)
Total volume variation (TVv)
Variation of the alveolar volume at the buccal and palatal side. The 3D-analysis was conducted with "Boolean" functions, which allowed researchers to obtain the volume variation in each time point from different variables like the Total Volume Variation (TVv0-1, TVv0-2, e TVv0-3), computed in cubic millimetres (mm3) and To allow a direct comparison of different sites at different time points, relative percentages of these variables were calculated based on the ROI volume at T0
Measured: Baseline (T0); 1 month (T1); 4 months (T2) and 12 months (T3)
Secondary outcomes (1)
Buccal wall thickness (BT)
measurement of the facial bone wall. The acquisition of radiographic images was performed with a volumetric dimension of 8 x 8 cm for 14s with the XG 3D tomography acquisition protocol, with a voxel size of 0.1 mm in HD mode. BT was measured 1 mm above the coronal bone margin using a central slice, as well at the mesial and distal slices, ranging 1 mm from the central slice. Mean BT values were obtained as the average values of the three slices. Measurements were made in mm.
Measured: baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Jun 2020
- Study start1 Jun 2019
- Primary completion8 Jun 2020
- Study completion8 Jun 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dental Implant FailedStudies 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
- 28 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universidade Católica Portuguesa
- Sponsor type
- University, hospital or other
- Collaborators
- Danilo Fernandes
- Responsible party
- Principal investigator, Tiago Borges, Universidade Católica Portuguesa
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04432519
- Sponsor's protocol ID
- 06.2019
- Status last verified
- Jun 2020
- First submitted
- 9 Jun 2020
- Last updated
- 16 Jun 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Jun 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Linear and Volumetric Analysis on the Effect of Customized Healing Abutments at Maxillary Immediate Implant Sites: a Prospective Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT04432519
- Acronym / sponsor ID
- 06.2019
- Conditions
- Dental Implant Failed
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 28 participants (actual)
- Lead sponsor
- Universidade Católica PortuguesaUniversity, hospital or other
- Collaborators
- Danilo Fernandes
- Study start
- 1 Jun 2019 (actual)
- Primary completion
- 8 Jun 2020 (actual)
- Study completion
- 8 Jun 2020 (actual)
- First posted
- 16 Jun 2020 (actual)
- 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.
Studies evaluating the use of customized healing screws/abutments in immediate implant placement have been performed, aiming to assess possible advantages with the use of this treatment modality. Despite the existence of these investigations, there is a lack of information regarding a digital approach to evaluate in an objective manner soft and hard tissue dimensional changes at this treatment modality.
Detailed description
Studies evaluating the use of customized healing screws/abutments have been performed aiming to assess possible advantages with the use of this treatment modality. Despite the existence of these investigations, there is a lack of information regarding a digital approach to evaluate in an objective manner soft and hard tissue dimensional changes.
The aim of this study is to perform a volumetric analysis evaluating peri-implant tissues dimensional changes on the effect of using customized healing abutments compared with the use of collagen matrices as socket sealing options in maxillary immediate implant placement.
The present study was designed as a prospective, randomized, controlled clinical trial with a parallel-group design, to document the response of using a customized healing abutment in maxillary immediate implants. Twenty-eight consecutive patients in need of a single implant restoration in the maxillary arch following tooth extraction were included in this study.
All patients were treated with cylindrical shape implants (OsseoSpeed EV™, AstraTech Implant System, Dentsply Implants, Möhndal, Sweden) with a narrow diameter internal connection platform following the surgical sequence protocol provided by the manufacturer. The implant was placed in a correct three-dimensional position, engaging the palatal and apical bone to achieve high primary stability. (Buser et al. 2004) After implant insertion, a gap of at least 2 mm between the inner cortical buccal bone plate and the implant surface was filled with DBBM material (Symbios®, Dentsply Implants, Möhndal, Sweden).
The two groups differ in the type of socket sealing. Control group fresh sockets were sealed with a resorbable collagen membrane (Mucograf Seal®, Geistlish Biomaterials, Wolhusen, Switzerland) stabilised with single interrupted 6/0 polyamide sutures (SeralonTM, Serag-Wiessner, Nalia, Germany), whereas test group received a healing abutment customized with a composite resin material allowing to close the socket without sutures.
Clinical examination and image acquisition Examination protocol and data collection consisted of four appointments: 1) T0 (flapless tooth extraction and implant insertion; 2) T1 (1-month follow-up after implant placement; 3) T2 (4-month follow-up after implant insertion) and 4) T3 (1-year postoperative follow-up). An intraoral scan of the upper arch (Cerec Omnicam®, Sirona Dental Systems GmbH, Bensheim, Germany) and a CBCT radiographic evaluation (Ortophos XG 3D®, Sirona Dental Systems GmbH, Bensheim, Germany) were performed followed by tooth extraction and implant placement (T0). At this point, two clinical parameters were assessed with a periodontal probe to the nearest millimetre: BID (distance between implant shoulder and the buccal bone plate) and KM (distance between the gingival groove and the mucogingival junction). Intraoral scans were completed post-implant placement at one month (T1), four months (T2) and twelve months (T3). In all follow-up appointments hygiene instructions were given to the patients and a periodontal care was executed when necessary.
Matching digital models All digital models were exported from the intraoral scanner in STL format. The T0 and T1, T0 and T2, and T0 and T3 STL files were overlapped and a strict alignment was made into one common coordinate system. A final alignment was done through the best fit alignment algorithm for a perfect match of digital models and executed with settings adjusted to the oral cavity.
After the superimposition of digital models, a colour map was created to quantitatively analyse the three-dimensional changes occurring in the surgical areas and adjacent tissues. Green areas correspond to the perfect alignment of the model. The variation between yellow and red represents variations of volumetric increase, whereas the variations between light blue and dark blue represent the variations of volumetric decrease. A region of interest (ROI) with 10 section planes, perpendicular to the coronal section of the tooth, was computed at buccal and palatal aspect (Figure 2). These sections were set at the most apical point of the gingival margin and ended 5 mm above it. Mesially and distally, a line passing through the interproximal area limited the region of interest. The same ROI was used in each patient, at the different comparison points. The intersection of these sections with the overlapping models allowed the linear changes to be obtained in each area. The Mean Buccal Change (MBC0-1, MBC0-2, and MBC0-3) and Mean Total Change (MTC0-1, MTC0-2 and MTC0-3) were calculated in millimetres (mm) to evaluate the changes that occurred in peri-implant contour (Figure 3).
Digital models superimposed in Geomagic Control X® were exported to Materialise Magics® for volumetric assessment. A volumetric ROI was manually selected with "Cut or Punch" function using interproximal areas as mesial and distal limits. All cuts were performed in the same way in all digital models so that all measurements were carried out in the same areas. ROI volume at T0 was computed for further comparison with consecutive volume variation values (Figure 4). The 3D-analysis was conducted with "Boolean" functions, which allowed researchers to obtain the volume variation in each time point from different variables like the Buccal Volume Variation (BVv0-1, BVv0-2, and BVv0-3) and Total Volume Variation (TVv0-1, TVv0-2, e TVv0-3), computed in cubic millimetres (mm3). To allow a direct comparison of different sites at different time points, relative percentages of these variables were calculated based on the ROI volume at T0 (Szathvary et al. 2015). All measurements were recorded to the nearest 0.01 mm.
Radiographic assessment The acquisition of radiographic images was performed with a volumetric dimension of 8 x 8 cm for 14s with the tomography acquisition protocol, with a voxel size of 0.1 mm in HD mode. The CBCT images were imported in a DICOM format to Mimics® software to perform the measurements. Buccal plate thickness (BT) was assessed for 3D radiographic analysis to evaluate the initial features of the alveolar bone. All measurements were obtained through coronal slice reconstructions, using an adjacent line to the sinus/nasal plate as a reference (Figure 5). BT was measured 1 mm above the coronal bone margin using a central slice, as well at the mesial and distal slices, ranging 1 mm from the central slice. Mean BT values were obtained as the average values of the three slices. One independent examiner who was not involved in the study executed all measurements.
Statistical analysis The outcome variables were presented as mean values, standard deviation, median and 95% confidence interval. Measurement time (T1, T2 and T3) was considered as a factor and the following as covariates: age, gender, KM height, location, implant length, BID and BT. The statistical analysis was performed using SPSS™ Statistical Package for the Social Sciences, version 21.0 (IBM Corporation, Armonk, NY, USA). The Mann-Whitney U-test was used to disclose differences for continuous non-paired variables. Moreover, the paired Wilcoxon test was used when the normal distribution of the groups was proved. A multiple linear regression model, using the stepwise forward method, was built to analyse the effect of the tested treatment in the main outcome variables throughout the study. All hypothesis tests were conducted at the 5% level of significance.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group CA | Experimental | Procedure: Immediate dental implant placementCustomized healing abutment inserted in immediate implant placement. |
| Group CM | Active comparator | Procedure: Immediate dental implant placementResorbable Collagen Membrane for socket closure in immediate implant placement. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- patients with ≥18 years of age;
- patients who had a failing tooth and needed an implant placing therapy in the aesthetic zone (between 15-25);
- the failing tooth has adjacent and opposing natural teeth;
- sufficient mesial-distal and inter-occlusal space for placement of the implant and definitive restoration;
- had an intact socket wall previously to the extraction;
Key exclusion criteria (3 listed)
- individuals diagnosed with periodontal disease;
- medical and general contraindications for the surgical procedure;
- heavy smokers (> 10 cigarettes/day); .an active infection at the implant site.
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 |
|---|---|---|
| Immediate dental implant placementAlso: Post extraction immediate implant placementDental implant insertion in the same surgical stage of the tooth extraction, consisting in implant placement in the fresh socket. | Procedure or surgery | Group CA, Group CM |
Primary outcome
Buccal volume variation (BVv)
Time frame: Baseline (T0); 1 month (T1); 4 months (T2) and 12 months (T3)
Variation of the alveolar volume at the buccal aspect. The 3D-analysis was conducted with "Boolean" functions, which allowed researchers to obtain the volume variation in each time point from different variables like the Buccal Volume Variation (BVv0-1, BVv0-2, and BVv0-3), computed in cubic millimetres (mm3) and To allow a direct comparison of different sites at different time points, relative percentages of these variables were calculated based on the ROI volume at T0.
Total volume variation (TVv)
Time frame: Baseline (T0); 1 month (T1); 4 months (T2) and 12 months (T3)
Variation of the alveolar volume at the buccal and palatal side. The 3D-analysis was conducted with "Boolean" functions, which allowed researchers to obtain the volume variation in each time point from different variables like the Total Volume Variation (TVv0-1, TVv0-2, e TVv0-3), computed in cubic millimetres (mm3) and To allow a direct comparison of different sites at different time points, relative percentages of these variables were calculated based on the ROI volume at T0
1 secondary outcome
Buccal wall thickness (BT)
Time frame: baseline
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 16 Jun 2020.
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Immediate dental implant placement in people with Dental Implant Failed, run by Universidade Católica Portuguesa at 1 site in Portugal.
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 3 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 16 Jun 2020. 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 Portugal. 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?
Buccal volume variation (BVv) (time frame: Baseline (T0); 1 month (T1); 4 months (T2) and 12 months (T3)). The study lists 2 primary outcomes in all. 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 16 Jun 2020.