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Clinical Trials/NCT04367766
NCT04367766
Recruiting
Not Applicable

Management of the Fresh Extraction Socket in the Aesthetic Area: Alveolar Ridge Preservation vs Immediate Implant Placement vs Delayed Implant Placement

Centro Specialistico Odontoiatrico, Rome1 site in 1 country60 target enrollmentSeptember 27, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tooth Extraction Status Nos
Sponsor
Centro Specialistico Odontoiatrico, Rome
Enrollment
60
Locations
1
Primary Endpoint
Rate of adjunctive bone and soft tissue augmentation procedures need.
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

After atraumatic tooth extraction and the assessment of the feasibility of immediate implant placement, patients will be randomly assigned to one of three treatment concepts:

  1. Immediate Implant Placement and Immediate Provisionalization
  2. Alveolar Ridge Preservation. After 4 months of healing an implant will be placed with simultaneous GBR and/or Soft Tissue Augmentation procedures, if needed.
  3. Spontaneous Healing of the socket. After 4 months of healing, an implant will be placedwith simultaneous GBR and/or Soft Tissue Augmentation procedures, if needed.

In all groups, four months after implant placement, a prosthesis will be delivered. From this experimental period onward, patients will be scheduled for maintenance. Clinical, radiographic and volumetric assessment will be performed by clinicians not involved in the surgery and blind with respect to treatment assignment at 1, 3 and 5 years post loading.

Detailed Description

The overall objective of this study will be to compare the three treatment modalities after tooth extraction (immediate implant placement, alveolar ridge preservation, spontaneous healing) in terms of: * patient-related (morbidity) outcomes during surgical procedure and the first 2 weeks after the surgical procedure * cost-effectiveness ratio (treatment time, number of surgeries, number of appointments and overall appointments time, need for bone and soft tissue augmentation, overall costs) at the time of prosthesis delivery * volumetric bone and soft tissue changes of the site before treatment (prior to tooth extraction), 4 months after tooth extraction, 1, 3 and 5 years after final prosthesis. * clinical, radiographic, aesthetic and patient-related (satisfaction) outcomes at the time of prosthesis delivery and 1, 3 and 5 years after final prosthesis. * Implant Success and Survival at 1, 3 and 5 years after final prosthesis.

Registry
clinicaltrials.gov
Start Date
September 27, 2023
End Date
August 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Centro Specialistico Odontoiatrico, Rome
Responsible Party
Principal Investigator
Principal Investigator

Marco Clementini

Research Fellow

Centro Specialistico Odontoiatrico, Rome

Eligibility Criteria

Inclusion Criteria

  • single tooth extraction in the anterior region of the dentition (including premolars) to be extracted
  • smoking no more than 10 cigarettes/day,
  • periodontal health (BoP \< 10%) and good plaque control (\< 20%)
  • absence of symptomatic periapical radiolucencies, acute abscesses at the site of extraction,
  • extraction sites with less than 30% loss of one or more walls
  • adequate quantity and quality of native bone to achieve primary stability

Exclusion Criteria

  • growing patients
  • patients with autoimmune disease, uncontrolled diabetes or immunocompromised
  • history of head and neck radiation for cancer treatment,
  • pregnancy

Outcomes

Primary Outcomes

Rate of adjunctive bone and soft tissue augmentation procedures need.

Time Frame: during implant placement

Number of participants with the need for adjunctive reconstructive hard tissue procedure during implant placement will be evaluated as a frequency (Yes/No) after a digital prosthetically driven implant placement. The need for soft tissue augmentation during implant placement will be evaluated as a frequency (Yes/No) by a blinded examiner in case of buccal soft tissue thickness \< 2mm assessed at 3mm apical to the full thickness flap margin with a caliber.

Secondary Outcomes

  • Peri-Implant Health(1, 3, 5 years post loading)

Study Sites (1)

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