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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04999956
Other study ID # SH9H-2020-T122-2
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 1, 2021
Est. completion date July 31, 2023

Study information

Verified date June 2023
Source Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Prosthetic-driven immediate implant placement for optimal aesthetic restoration has been increasing in demand during the last decades but requires higher accuracy. Dynamic navigation has been reported better implant positioning. However, dynamic navigation's application to immediate implant placement has not been studied, and its exact role is still needed to be investigated further. Besides, implant insertion angle may influence primary stability, which is a prerequisite in achieving osseointegration, while dynamic navigation can precisely control angle and position. Therefore, the investigators designed a randomized controlled clinical trial study to verify the clinical efficacy of dynamic navigation and freehand in immediate implant placement. Patients will then be followed up one year after delivery of the crown to assess additional parameters.


Description:

Prosthetic-driven immediate implant placement for optimal aesthetic restoration has been increasing in demand during the last decades but requires higher accuracy. Dynamic navigation has been reported better implant positioning. However, dynamic navigation's application to immediate implant placement has not been studied, and its exact role is still needed to be investigated further. Besides, implant insertion angle may influence primary stability, which is a prerequisite in achieving osseointegration, while dynamic navigation can precisely control angle and position. Therefore, the investigators designed a randomized controlled clinical trial study to verify the clinical efficacy of dynamic navigation and freehand in immediate implant placement. Patients will then be followed up one year after delivery of the crown to assess additional parameters. These will include the assessment of soft tissue inflammation, cytokine concentrations, microbiome, stability of the buccal bone plate.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 24
Est. completion date July 31, 2023
Est. primary completion date December 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. =18 years old and in good health; 2. The maxillary incisor that cannot be retained due to non-periodontitis; 3. The buccal bone plate is complete; 4. No acute infection; 5. The extraction socket have at least 3-5 mm apical bone. Exclusion Criteria: 1. General contraindications of oral implant surgery (such as immunodeficiency, long-term use of corticosteroids); 2. Treatments or diseases that may affect bone tissue metabolism (for example, taking bisphosphonates or receiving local radiotherapy); 3. Periodontitis history or uncontrolled periodontitis. Bleeding of probing (BOP) positive site = 10%, or probing depth (PD) = 4mm; 4. Heavy smokers or previous heavy smoking history (quit smoking time <5 years or> 20 cigarettes per day); 5. Refuse to participate in this trial.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
dynamic navigation surgery
immediate implant placement using dynamic navigation
freehand surgery
immediate implant placement using freehand surgery

Locations

Country Name City State
China Department of Oral and Maxillo-facial Implantology, Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiaotong University Shanghai Shanghai
China Department of Oral and Maxillofacial Implantology Shanghai Shanghai
China Shanghai Ninth People's Hospital Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Accuracy Taking cone-beam computed tomography (CBCT). The deviation between the planned implant and the actual implant were measured by Computer Assisted Dental Implant Precision System (Dcarer, Suzhou, China) as follows: (1) At least four feature points (like tooth cusps or bone pits) were selected in preoperative and postoperative CBCT for rough registration. (2) Feature surface circles in preoperative CBCT were selected, and then a mathematical algorithm displayed a similar feature surface circle in postoperative CBCT. The algorithm registered thousands of points in these two circles via conventional iso-surface thresholding technology. The software calculated registration error automatically. (3) Finally, the planned and actual implant were identified, and the deviation would be automatically calculated. before surgery to after surgery one week
Primary Peri-implant soft tissue health Assessment of tissue health according to the definition of the 2017 International Classification. Berglundh et al. 12-months follow-up after delivery of crown
Secondary Insetion torque value (ITV) A general method to to detect primary stability roughly. The ITV were evaluated by a wrench (Straumann, Waldenburg, Switzerland) at the time of implant placement. The investigator record the number of scale. Being equal to or greater than 35N is a ideal primary stability. surgery day
Secondary Implant Stability Quotient (ISQ) A device to detect primary stability precisely. A Smartpeg was screwed into each implant, and resonance frequency analysis (RFA) was performed using Osstell Mentor (Osstell/Integration Diagnostics, Goteborg, Sweden). ISQ were recorded in the buccal and the palatal directions three times and averaged. <60 represents low stability; 60-70 represents medium stability; higher than 70 represents high stability. surgery day
Secondary Esthetic appearance of the dental crown PES-WES Score assessed using the Belser criteria 12-months follow-up after delivery of the crown
Secondary Patient satisfaction Assessed using a visual analogue scale (VAS=100mm, with 0=completely dissatisfied and 100 completely satisfied). 12-months follow-up after delivery of crown
Secondary Peri-implant sulcus fluid Inflammation Cytokine concentrations determined by multiplex ELISA 12-months follow-up after delivery of crown
Secondary Buccal bone changes Measurements performed on post-operative CBCT taken for routine follow-up 12-months follow-up after delivery of crown
Secondary Implant microbiome 16S microbiome analysis performed on submarginal biofilm taken with a sterile paper point 12-months follow-up after delivery of crown
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