Edentulous Alveolar Ridge Clinical Trial
Official title:
Long-term Dimensional Changes in Single Crowns Supported by Short (6 mm) Transmucosal Implants With Divergent or Convergent Neck Profiles in the Esthetic Zone. A Randomized Randomized Controlled Clinical Trial
The goal of the present randomized clinical trial is to assess the long-term osseous and peri-implant soft tissue changes as well as the success rate of short implants (6 mm) with a converging collar with micro threads or a diverging polished collar placed in the esthetic zone of the maxilla on partially edentulous patients. The main questions it aims to answer are: - what are the long-term bone and soft tissue changes around implants with a converging collar with micro threads compared to a diverging polished collar placed in the esthetic zone of the maxilla? - What is the success rate of implants with a converging collar with micro threads compared to a diverging polished collar placed in the esthetic zone of the maxilla? Dental implants with a converging collar with micro threads or a diverging polished collar will be placed in the esthetic zone of the maxilla of the included participants and the measurements regarding the bone and soft tissue level will be compared.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | December 30, 2026 |
Est. primary completion date | December 30, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years to 60 Years |
Eligibility | Inclusion Criteria: - Presence of at least two edentulous areas in the esthetic region of the maxilla (from right to left from second premolar to premolar, preferably first premolars and incisors) - Alveolar bone = 8 mm in height and = 5 mm in thickness assessed on CBCT. - Age of = 21 years. - Need for an implant-supported prosthetic restoration. - Be in good general health with no contraindications to oral surgical procedures. - Not be pregnant. - Patients who agree to participate in the study and sign the informed consent. Exclusion Criteria: - The presence of any uncontrolled systemic disease. - History of past or ongoing chemotherapeutic or radiotherapeutic treatments. - Heavy smokers (>10 cigarettes per day). - Previous bone regeneration procedures in the area of interest |
Country | Name | City | State |
---|---|---|---|
Peru | Universidad Nacional de Trujillo | Trujillo | La Libertad |
Lead Sponsor | Collaborator |
---|---|
ARDEC Academy | Universidad Nacional de Trujillo |
Peru,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | height of the periimplant bone tissues | The height of the periimplant bone tissues will be evaluated in the intraoral radiographic images, cone beam tomography, and the three-dimensional images obtained from the digital prints | baseline | |
Primary | height of the periimplant bone tissues | The height of the periimplant bone tissues will be evaluated in the intraoral radiographic images, cone beam tomography, and the three-dimensional images obtained from the digital prints | 3 years follow up | |
Primary | height of the periimplant soft tissues | The height of the periimplant soft tissues will be evaluated in the intraoral radiographic images, cone beam tomography, and the three-dimensional images obtained from the digital prints | Baseline | |
Primary | height of the periimplant soft tissues | The height of the periimplant soft tissues will be evaluated in the intraoral radiographic images, cone beam tomography, and the three-dimensional images obtained from the digital prints | 3 years follow up | |
Secondary | Plaque index | to score the plaque accumulation of plaque around implants will be used the Mombelli et al index | 1 year | |
Secondary | Plaque index | to score the plaque accumulation of plaque around implants will be used the Mombelli et al index | 3 year | |
Secondary | Bleeding on probing | During the probing, the bleeding on probing will be registered in the periodontal record. | 1 year | |
Secondary | Bleeding on probing | During the probing, the bleeding on probing will be registered in the periodontal record. | 3 year | |
Secondary | Probing depth | A calibrated probe will be used to measure the probing depth in all teeth annually. | 1 year | |
Secondary | Probing depth | A calibrated probe will be used to measure the probing depth in all teeth annually. | 3 year | |
Secondary | Implant success rate | The criteria to evaluate the success rate will be if there was no persistent and/or irreversible signs or symptoms such as pain, infection, neuropathies, or paresthesia, no peri-implant infection with suppuration, no mobility, and no continuous radiolucency around the implant. | 1 year | |
Secondary | Implant success rate | The criteria to evaluate the success rate will be if there was no persistent and/or irreversible signs or symptoms such as pain, infection, neuropathies, or paresthesia, no peri-implant infection with suppuration, no mobility, and no continuous radiolucency around the implant. | 3 years |
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