The Use of a Porcine Collagen Matrix for the Prevention of Buccal Bone Wall Resorption During Implant Placement in the Aesthetic Zone.

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorAristotle University Of Thessaloniki

About this trial

Aim:

To provide a comparative assessment of the clinical and radiographic effect of porcine collagen matrix when placed buccally at the time of single implant placement in the aesthetic zone vs autogenous connective tissue graft in terms of buccal bone resorption and soft tissue augmentation 6 months post operative. Histological assessment and patient reported outcomes were reported

Eligibility criteria

Qualifiers

Generally healthy adult patients.

18 years or older.

Need for replacement of single implant in the upper aesthetic zone (second premolar to second premolar)

Ridge width (bucco-lingual) no greater than 6 mm at its narrowest point.

Disqualifiers

Poor oral hygiene (FMPS < 20%, FMBS < 15%) and poor motivation

Heavy smokers (>10 cigarettes per day)

Need for bone augmentation

Untreated periodontitis

Trial design

Treatments tested in this trial

  • CTG
  • Collagen Matrix
  • Control group

Treatment groups

36 Participants
are divided into 3 treatment groups