Immediate Versus Delayed Loading of Single Posterior Zirconia Implants: A Multicenter Randomized Controlled Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Sistemically healthy patients

• partial edentulism

• premolar position

• molar position

• Bone width and height at least 6 and 10mm, respectively.

• Keratinized tissue, at least 1 mm at implant site

• Full understanding of the proposed surgical treatments and the protocol schedule

• Full comprehension and availability to sign the informed consent form

Locations
Other Locations
Italy
San Paolo Hospital
RECRUITING
Milan
Time Frame
Start Date: 2022-12-01
Estimated Completion Date: 2029-06-01
Participants
Target number of participants: 220
Treatments
Experimental: Immediate loading zirconia implant
Loading of zirconia dental implant within 7 days after implant placement
Active_comparator: Delayed loading zirconia implant
Loading of zirconia dental implants after at least 2 months of healing
Related Therapeutic Areas
Sponsors
Leads: University of Milan

This content was sourced from clinicaltrials.gov