Clinical Trial

Socket Reconstruction Technique and Immediate Implant Placement With Two Different Bone Substitute Materials.

Recruiting
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Record status
This record was last updated April 16, 2025 (before its estimated June 2025 completion). Its status may not reflect the trial's current state.
Summary
The present research is a national multicentric prospective parallel double-blinded (both the patient and the examiner are blind) randomized controlled clinical trial. It is a superiority comparative study on a medical device CE (conformité européenne) marking, used according to the intended use subject to the CE marking. The hypothesis tested is: the socket reconstruction procedure performed in conjunction with Immediate implant placement (IIP) with the use of Deproteinized bovine bone mineral + hyaluronic acid (DBBM+HA, Cerabone plus) leads to a greater increase in the vertical buccal bone height than same procedure with deproteinized bovine bone mineral alone (DBBM, Bio-oss Collagen).
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-07-17.
Status change: Not Yet Recruiting → Recruiting 2025-04-12
Trial Details
NCT Number NCT06517030
Lead Sponsor Università Vita-Salute San Raffaele
Conditions Dental Implant
Enrollment 30 participants
Start Date 2025-04
Primary Completion 2025-06 (estimated)
Study Completion 2025-09 (estimated)
Updated on ClinicalTrials.gov 2025-04-16