ISQ Differences Between Different Implants in Post-extraction Sockets
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-99
SponsorUniversity of Rome Tor Vergata
About this trial
Two different implants will be used in post-extraction sockets and ISQ will be recorded monthly from insertion moment to 12 months of follow up to understand if ISQ can be affected by implant macro design
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients (at least 18 years old) presenting with failing tooth.
no recession of gingival contour of tooth to be extracted
no periodontal bone loss of neighboring teeth
no implants in neighboring teeth
Disqualifiers
deep bite (severe II class)
systemic disease (diabetes, osteoporosis)
heavy smokers (more than 10 cigarettes/day)
Trial design
Design model
Parallel
Treatments tested in this trial
Implant stability quotient
Diagnostic testScrew a smart peg into the implant and record the values from a dedicated device
Treatment groups
30 Participants
are divided into 2 treatment groupsGroup A: TISSUE LEVEL XActive comparator 1 intervention
Group B: TISSUE LEVEL CExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
IMPLANT STABILITY QUOTIENT
Values of risonance of implants taken by means of a dedicated device that translate the risonance of each implant into a number (0-99).
Time frame
Monthly from T0 (implant insertion) to T12 (12 months after implant placement)Secondary outcomes
1
Insertion torque
Mechanical resistance of the bone at implant placement
Time frame
At implant placementSponsors and contacts
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Source ClinicalTrials.gov