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Dimensional Changes in Single Crowns Supported by Short Transmucosal Implants With Diverging or Converging Neck Profiles in the Esthetic Zone

Primary Purpose

Edentulous Alveolar Ridge

Status
Recruiting
Phase
Not Applicable
Locations
Peru
Study Type
Interventional
Intervention
Dental implants placement
Sponsored by
ARDEC Academy
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Edentulous Alveolar Ridge focused on measuring Maxilla, Partially edentulous, Dental implant, Implant supported prosthesis

Eligibility Criteria

21 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Universidad Nacional de TrujilloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

dental implant with a convergent collar

dental implant with a divergent collar

Arm Description

One implant with a converging collar with micro threads will be installed in each patient according to the site randomization in the esthetic region of the upper jaw (between the second premolars).

One implant with a diverging polished collar will be installed in each patient according to the site randomization in the esthetic region of the upper jaw ( between the second premolars).

Outcomes

Primary Outcome Measures

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
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
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
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

Secondary Outcome Measures

Plaque index
to score the plaque accumulation of plaque around implants will be used the Mombelli et al index
Plaque index
to score the plaque accumulation of plaque around implants will be used the Mombelli et al index
Bleeding on probing
During the probing, the bleeding on probing will be registered in the periodontal record.
Bleeding on probing
During the probing, the bleeding on probing will be registered in the periodontal record.
Probing depth
A calibrated probe will be used to measure the probing depth in all teeth annually.
Probing depth
A calibrated probe will be used to measure the probing depth in all teeth annually.
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.
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.

Full Information

First Posted
April 5, 2023
Last Updated
August 18, 2023
Sponsor
ARDEC Academy
Collaborators
Universidad Nacional de Trujillo
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1. Study Identification

Unique Protocol Identification Number
NCT06006156
Brief Title
Dimensional Changes in Single Crowns Supported by Short Transmucosal Implants With Diverging or Converging Neck Profiles in the Esthetic Zone
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
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2023 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ARDEC Academy
Collaborators
Universidad Nacional de Trujillo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
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.
Detailed Description
The objectives of the present randomized clinical trial are to evaluate the clinical and radiographic changes over time of hard and soft tissues around implants with a convergent or divergent collar. Twenty volunteer participants with two edentulous regions in the maxillary esthetic zone (from the right second premolar to the left second premolar) will be included in the study. Two implants will be randomly installed, one with a convergent collar and one with a divergent collar. After 3 months of healing, individual crowns will be installed. At each visit the following parameters will be evaluated: plaque index, probing depth, bleeding on probing, the recession of the mucosal margin, intraoral radiographs, likewise control CBCT, and impressions will be performed. The visit will take place at 6 and 12 months and then annually for a minimum of 3 years. Changes at the level of the marginal bone will be assessed overtime on the radiographs. Dimensional changes will be clinically evaluated during control evaluations and later through digital impressions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Edentulous Alveolar Ridge
Keywords
Maxilla, Partially edentulous, Dental implant, Implant supported prosthesis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is a split-mouth randomized controlled trial. One implant with a converging collar with micro threads or a diverging polished collar will be installed in each patient according to randomization in the esthetic region of the upper jaw ( between the second premolars ). It will be restored with individual crowns after three months of healing. Both implants will be placed with the rough margin of ~1 mm subcrestally.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Treatment assignments will be sealed in opaque envelopes that will be opened during the surgery. The treatment assignment will be disclosed to the surgeon after the elevation of the alveolar mucosal flaps and prior to the preparation of the recipient sites.
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
dental implant with a convergent collar
Arm Type
Experimental
Arm Description
One implant with a converging collar with micro threads will be installed in each patient according to the site randomization in the esthetic region of the upper jaw (between the second premolars).
Arm Title
dental implant with a divergent collar
Arm Type
Active Comparator
Arm Description
One implant with a diverging polished collar will be installed in each patient according to the site randomization in the esthetic region of the upper jaw ( between the second premolars).
Intervention Type
Procedure
Intervention Name(s)
Dental implants placement
Other Intervention Name(s)
dental implant installation, implant supported prosthetic restoration
Intervention Description
Two one-piece trans gingival implants, One with a convergent hyperbolic collar, and one with a divergent profile collar will be used.
Primary Outcome Measure Information:
Title
height of the periimplant bone tissues
Description
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
Time Frame
baseline
Title
height of the periimplant bone tissues
Description
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
Time Frame
3 years follow up
Title
height of the periimplant soft tissues
Description
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
Time Frame
Baseline
Title
height of the periimplant soft tissues
Description
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
Time Frame
3 years follow up
Secondary Outcome Measure Information:
Title
Plaque index
Description
to score the plaque accumulation of plaque around implants will be used the Mombelli et al index
Time Frame
1 year
Title
Plaque index
Description
to score the plaque accumulation of plaque around implants will be used the Mombelli et al index
Time Frame
3 year
Title
Bleeding on probing
Description
During the probing, the bleeding on probing will be registered in the periodontal record.
Time Frame
1 year
Title
Bleeding on probing
Description
During the probing, the bleeding on probing will be registered in the periodontal record.
Time Frame
3 year
Title
Probing depth
Description
A calibrated probe will be used to measure the probing depth in all teeth annually.
Time Frame
1 year
Title
Probing depth
Description
A calibrated probe will be used to measure the probing depth in all teeth annually.
Time Frame
3 year
Title
Implant success rate
Description
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.
Time Frame
1 year
Title
Implant success rate
Description
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.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Daniele Botticelli, PhD
Phone
+393339070450
Email
daniele.botticelli@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Karol Ali Apaza alccayhuaman, PhD
Phone
+436769178911
Email
karol.ali.apazaa@gmail.com
Facility Information:
Facility Name
Universidad Nacional de Trujillo
City
Trujillo
State/Province
La Libertad
ZIP/Postal Code
13001
Country
Peru
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Miguel Ccarhuayo Matta, PhD
Phone
+51949434377
Email
miguelcarhuayo@icloud.com

12. IPD Sharing Statement

Plan to Share IPD
No
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Dimensional Changes in Single Crowns Supported by Short Transmucosal Implants With Diverging or Converging Neck Profiles in the Esthetic Zone

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