Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05315414
Other study ID # C-PT-21-001
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 3, 2022
Est. completion date May 2029

Study information

Verified date June 2024
Source Dentsply Sirona Implants and Consumables
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the clinical outcome of implant survival of the PrimeTaper EV implant in single tooth restorations 1 year after permanent restoration.


Other known NCT identifiers
  • NCT05387421

Recruitment information / eligibility

Status Active, not recruiting
Enrollment 138
Est. completion date May 2029
Est. primary completion date May 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Adult aged 18-75 years. - Willing and able to sign and date the informed consent form. - In need of an implant in position 16 to 26 or 36 to 46, and each subject can only receive one implant. - Deemed by the investigator as likely to present with an initially stable implant situation. - A stable occlusion, i.e. an opposing natural dentition, a crown, an implant-supported fixed or removable prosthesis, a partial removable prosthesis or a full denture. - An adjacent tooth (root with natural or artificial crown) or an implant-supported crown mesially and distally. Exemption: If the planned implant is in the first molar position, an edentulous space is accepted distally Exclusion Criteria: - Not willing to participate in the clinical investigation or not able to understand the content of the clinical investigation. - Unlikely to be able to comply with clinical investigation procedures according to investigator's judgement. - Unable or unwilling to return for follow-up visits for a period of 5 years. - Known allergy or hypersensitivity to titanium and/or stainless steel. - Uncontrolled pathological process in the oral cavity, e.g. untreated rampant caries and uncontrolled periodontal disease. - Uncontrolled para-functional habits, e.g. bruxism. - Current need of any Guided Bone Regeneration (GBR) procedure in the planned implant area (gap filling at immediate placement and soft tissue grafting are allowed). - Systemic or local disease or condition that would compromise post-operative healing and/ or osseointegration. - Immunosuppression, use of corticosteroids, per-os or intravenous bisphosphonate use, or any other medication such as anti-resorptive therapy or monoclonal antibodies that could compromise post-operative healing and/or osseointegration. - Any other condition that would make the subject unsuitable for participation, including but not limited to; - History of radiation therapy in the head and neck region. - History of chemotherapy within 5 years prior to surgery. - Present alcohol and/or drug abuse. - Ongoing psychiatric illness. - Current smoking/use of tobacco, including e-cigarettes. - Any ongoing disease that would make the subject unsuitable for participation, including but not limited to; - Recent myocardial infarction (< 3 months*). - Recent cerebrovascular accident (< 3 months*). - Recent cardiac-valvular prosthesis placement (< 3 months*). - Hemorrhagic diathesis. - Severe liver dysfunction. - Known or suspected current malignancy. - Uncontrolled diabetes mellitus. - Florid infection. - Pregnant or breastfeeding females. (Pregnancy tests will be performed as per local requirements). - Previous enrolment in the present clinical investigation. - Involvement in the planning and conduct of the clinical investigation (applies to both Dentsply Sirona staff and the clinical investigation site). - Simultaneous participation in another clinical investigation, or participation in a clinical investigation during the last 6 months that may interfere with the present clinical investigation. - < 3 months is a strict exclusion criterion. After 3 month it is up to the investigator to judge whether the subject is considered suitable for participation or not.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
PrimeTaper EV implant
Tapered dental implant developed by Dentsply Sirona

Locations

Country Name City State
Belgium Catholic University of Leuven Leuven
Germany Dental practice Dr Mischa Krebs Alzey
Italy Studio Toia Busto Arsizio
Netherlands Dr.F.L.Guljé, De Mondhoek Apeldoorn
United States University of Iowa Iowa City Iowa

Sponsors (1)

Lead Sponsor Collaborator
Dentsply Sirona Implants and Consumables

Countries where clinical trial is conducted

United States,  Belgium,  Germany,  Italy,  Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Implant survival, i.e. number of implants in place counted clinically, 1 year after permanent restoration. Implant survival rate is a binary variable evaluated clinically, i.e. 'Yes' or 'No' where 'Yes' means that the implant is still in place and 'No' means that the implant is not in place. Any implant that has been removed or lost after implant placement visit will be considered a failure, whatever the reason for removal/loss. One year post permanent restoration (anticipated average 3 months after implant placement).
Secondary Implant survival, i.e. number of implants in place counted clinically, 2, 3, 4 and 5 years after permanent restoration. Implant survival rate is a binary variable evaluated clinically, i.e. 'Yes' or 'No' where 'Yes' means that the implant is still in place and 'No' means that the implant is not in place. Any implant that has been removed or lost after implant placement visit will be considered a failure, whatever the reason for removal/loss. 2, 3, 4 and 5 years post permanent restoration (anticipated average 3 months after implant placement).
Secondary Change of implant stability quotient value (ISQ) between implant placement and permanent restoration. Implant stability will be evaluated through ISQ value using Resonance Frequency Analysis (RFA). The stability is presented as an ISQ value. The higher the ISQ value the higher the stability. Recorded as a numeric value (1-100). From date of implant placement (anticipated average 1 month after inclusion) to date of permanent restoration (anticipated average 3 months after implant placement).
Secondary Maximum insertion torque value for each implant at implant placement. Maximum insertion torque value (ITV), based on ITV curve, measured in Ncm. At date of implant placement (anticipated average 1 month after inclusion).
Secondary Final insertion torque value for each implant at implant placement. Final insertion torque value (ITV), based on ITV curve, measured in Ncm. At date of implant placement (anticipated average 1 month after inclusion).
Secondary Investigator questionnaire for each investigational medical device after implant placement. Numerical scale 1-10, where 1 = totally disagree with the statement, and 10 = totally agree with the statement. Statements to be evaluated by the surgeon: "The implant was guided into the prepared osteotomy", "The implant followed the prepared osteotomy", "The implant has a good primary stability", "The drilling protocol is easy to use", "The implant has efficient cutting properties". Each statement will be evaluated separately. Immediately after implant placement (anticipated average 1 month after inclusion).
Secondary Implant success, i.e., number of implants documented as successful at 1, 2, 3 and 5 years after permanent restoration. Successful implants counted, i.e. 'Yes' or 'No'. An implant will be considered successful if all of the following criteria are fulfilled:
Implant in place.
Lack of evidence of peri-implant radiolucency in X-ray.
Less than 1mm vertical bone loss during first year after loading with permanent restoration and 0,2mm annually thereafter.
Absence of persistent and/or irreversible signs and symptoms such as pain, infections, neuropathies, paresthesia, or violation of the mandibular canal.
1, 2, 3 and 5 years post permanent restoration (anticipated average 3 months after implant placement).
Secondary Change of marginal bone level up to 5 years post permanent restoration compared to permanent restoration. MBL changes determined from radiographs, expressed as the distance from the implant reference point to the most coronal bone-to-implant contact on the mesial and distal side of the implant. The average will be calculated and compared for each evaluation period. At permanent restoration (anticipated average 3 months after implant placement) and 1, 2, 3 and 5 years post permanent restoration.
Secondary Change of probing pocket depth (PPD) in mm between permanent restoration, and 6 months, 1, 2, 3, 4 and 5 years after permanent restoration. Probing Pocket Depth (PPD) measured as the distance from the mucosal margin to the bottom of the probe-able pocket in mm. At permanent restoration (anticipated average 3 months after implant placement) and 6 months, 1, 2, 3, 4 and 5 years post permanent restoration.
Secondary Presence of bleeding on probing (BoP), at permanent restoration, and 6 months, 1, 2, 3, 4 and 5 years after permanent restoration. Bleeding on Probing (BoP) recorded as presence or absence of bleeding when probing to the bottom of the pocket. At permanent restoration (anticipated average 3 months after implant placement) and 6 months, 1, 2, 3, 4 and 5 years post permanent restoration.
Secondary Presence of plaque at 6 months, 1, 2, 3, 4 and 5 years after permanent restoration. Plaque recorded as presence or absence of plaque by visual inspection on four surfaces at each implant site. 6 months, 1, 2, 3, 4 and 5 years post permanent restoration (anticipated average 3 months after implant placement).
Secondary Occurrence of Adverse Events, Adverse Device Effects, and Device Deficiencies during the clinical investigation. Adverse Events, Adverse Device Effects, and Device Deficiencies spontaneously reported, and collection at each clinical investigation visit. Up to 5 years after permanent restoration (anticipated average 3 months after implant placement).
See also
  Status Clinical Trial Phase
Recruiting NCT02880891 - Effects of Splinted or Non-splinted Single-unit Crowns on Marginal Bone-level Alterations Around Implants N/A
Completed NCT00748241 - Study to Evaluate Implant Survival Rate of Astra Tech Fixture ST in the Posterior Maxilla With One-stage Surgery and Early Loading N/A
Active, not recruiting NCT04066309 - Implant Retained Rehabilitation With Surgical and Prosthetic Digital Workflow N/A
Active, not recruiting NCT04545840 - Prospective Neodent® Zirconia System Study
Active, not recruiting NCT06034067 - Osseodensification Versus Conventional Drilling for Implant Site Preparation N/A
Active, not recruiting NCT04546269 - Fully Guided Versus Conventionally Guided Implant Placement by Dental Students N/A
Recruiting NCT02676661 - Evaluation of the Prevalence and Risk Factors for Patients With Peri-implant Disease N/A
Recruiting NCT02662361 - Evaluation of the Prevalence and Risk Factors for Patients With Peri-implant Diseaseļ¼ša Retrospective Study N/A
Completed NCT01030523 - Short Implants - An Alternative to Bone Grafting? N/A
Completed NCT00906425 - Clinical Study Comparing Submerged Versus Trans-mucosal Healing of P.004 Implants in the Anterior Mandible and Maxilla N/A
Completed NCT03252106 - Long-term Effectiveness of Contour Augmentation in Sites With Early Implant Placement N/A
Completed NCT02975674 - Evaluation of MT-12 Implant Survival and Marginal Bone Loss N/A
Completed NCT01822223 - A Study to Evaluate the Effectiveness of Laser-Ablated Implant-Abutments to Promote Tissue Healing N/A
Completed NCT00545818 - Study Comparing OsseoSpeedā„¢ Implants of Two Different Lengths in the Upper and Lower Posterior Jaw N/A
Completed NCT00900822 - Straumann Bone Ceramic Versus BioOss in Sinus Elevation N/A
Completed NCT04017026 - Survival and Success Rates of 6mm Implants With a Micro-rough Surface After 4.5 - 18.2 Years in Function
Recruiting NCT02814149 - Esthetic, Clinical and Radiographic Outcomes of Immediate and Delayed Implant Placement N/A
Active, not recruiting NCT03319758 - Esthetic and Radiographic Outcomes Following Immediate Implant Placement With Thin or Dehiscence Buccal Bone Wall N/A
Completed NCT01842958 - Straumann Roxolid Multi-Center Study N/A
Completed NCT01807416 - Bone Dimensional Changes at Different Implant-to-abutment Connections: a 1-year Clinical and Radiological Study Phase 4