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Immediate Load in Dental Implants Using Conventional Drilling and Piezoelectric Osteotomy on Aesthetic Zone.

Not Applicable
Conditions
Dental Implants
Tooth Loss
Interventions
Procedure: Piezoelectric osteotomy.
Procedure: Conventional drilling
Registration Number
NCT04497571
Lead Sponsor
Universidad de Granada
Brief Summary

Compare the survival rate of the implants placed using the ultrasonic technique and placed using conventional drilling, with an immediate load on the aesthetic zone.

Detailed Description

Main goals.

Compare the survival rate of the implants placed using the ultrasonic technique and placed using conventional drilling, with an immediate load on the aesthetic zone.

Specific goals.

* Evaluate the marginal peri-implant bone loss after the healing period through radiographs, from the day of surgery, to a month, to 3 and 6 months after and a year after the implants insertion.

* Evaluate the primary stability of each individual implant the day of their insertion to verify their load on the moment of surgery and also compare the values of each preparation techniques of implant bone preparation.

* Evaluate the secondary stability of each individual implant and compare the values of each preparation techniques.

* Evaluate the peri-implant clinic parameters within 3 and 6 months and a year after the insertion of the implants through these variables: probing depth and bleeding of probing.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Absence of teeth on the aesthetic zone, whether its an incisor, canine or premolar.
  • 3 months after the dental extraction without alveolar scar tissue remains.
  • Bone availability of at least 5mm of width and 13mm of length.
  • At least 2 to 3 mm of soft tissue for the establishment of an adequate peri-implant biological width.
  • Oclusal pattern that ensures prosthetic success.
  • Implants need to have at least a 35 N and 70 ISQ index to be loaded.
  • Index of plaque < 20% and/or inactive periodontal disease.
Exclusion Criteria
  • Acute myocardial infarction in the last 2 months.
  • Uncontrolled coagulation disorders
  • Uncontrolled diabetes (HbA1c> 7.5%).
  • Radiotherapy on head/neck in the last 24 months.
  • Immunocompromised patient.
  • History of medication related to osteonecrosis of the jaws.
  • Psychiatric disorders, alcohol, drugs and large smokers (>10 cigarrillos).
  • Plaque index > 20%.
  • Need for simultaneous or previous peri-implant guided bone regeneration procedures.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Piezoelectric osteotomyPiezoelectric osteotomy.Implant placement by piezoelectric osteotomy
Conventional drillingConventional drillingImplant placement by conventional drilling
Primary Outcome Measures
NameTimeMethod
Marginal Bone Loss12 months

To compare MBL measured using radiographs.

Secondary Outcome Measures
NameTimeMethod
Primary stabilityBaseline

Implant Stability Quotient Values (Osstell ISQ, Osstell USA) obtained from implants in study site, recording immediately.

Bleeding of probing3,6,12 months

Evaluate the peri-implant clinic parameters within 3 and 6 months and a year after the insertion of the implants through these variables: probing depth and bleeding of probing.

Secondary stability3 months

Implant Stability Quotient Values (Osstell ISQ, Osstell USA) obtained from implants in study site, recording at 3 months.

Survival rate3,6,12 months

To measure implant success rate.

Probing depth3,6,12 months

Evaluate the peri-implant clinic parameters within 3 and 6 months and a year after the insertion of the implants through these variables: probing depth and bleeding of probing.

Trial Locations

Locations (1)

Isabel Godoy Reina

🇪🇸

Almería, Spain

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