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Recruiting NCT06711744

ISQ Differences Between Different Implants in Post-extraction Sockets

No phase Interventional Bone Healing Implant Stability

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Implant stability quotient.
Who it may be relevant to
Registry conditions: Bone Healing, Implant Stability. Basic parameters: 18 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Effect of Time and Local Factors on Hydrophilic Tissue Level Implants in Post-extraction Sites: a RCT

Overview

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

Interventions

  • Diagnostic test Implant stability quotient
    Screw a smart peg into the implant and record the values from a dedicated device

Primary outcome measures

  • IMPLANT STABILITY QUOTIENT [Time frame: Monthly from T0 (implant insertion) to T12 (12 months after implant placement)]
Secondary outcome measures (1)
  • Insertion torque [Time frame: At implant placement]

Eligibility criteria

Inclusion criteria

  • 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
  • class I extraction socket (intact buccal wall)
  • atraumatic extraction of the tooth with intact socket walls remaining.

Exclusion criteria

  • deep bite (severe II class)
  • systemic disease (diabetes, osteoporosis)
  • heavy smokers (more than 10 cigarettes/day)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Diagnostic

Study locations

Italy · 1 center
  • Paolo Carosi — Rome

Identifiers

NCT: NCT06711744 · TLCVSTLX

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗