Immediate Versus Delayed Loading of Single Posterior Zirconia Implants

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversity of Milan

About this trial

The main aim of the present study is to investigate implant success rate after 5 years of function of immediate (Test group; within 7 days of implant placement) versus delayed (Control group; 8 weeks after implant placement) loading of two-pieces zirconia implant, placed in pristine bone without bone regeneration. Implant success rate will be defined according to Buser's criteria. Secondary endpoints: Marginal bone level (MBL) evaluation by means of standardized radiographs; Clinical evaluation of biological (e.g. Plaque Index, PI; Probing Pocket Depth, PPD, Bleeding on Probing, BOP; suppuration upon probing/palpation) and prosthetic/technical complications; Clinical evaluation of soft tissue width, keratinized tissue, marginal and interproximal soft tissue recession; Patient reported outcome measures (PROMs) by questionnaire administration:

Eligibility criteria

Qualifiers

Sistemically healthy patients

partial edentulism

premolar position

molar position

Disqualifiers

Heavy smokers (>10 cigarettes a day)

Serious kidney or liver diseases

Uncontrolled diabetes

Bisphosphonates intake

Trial design

Treatments tested in this trial

  • Zirconia implant

Treatment groups

220 Participants
are divided into 2 treatment groups

Sponsors and collaborators