Clinical Outcomes of Immediate Implants With or Without a Volume-stable Collagen Matrix
Clinical Outcomes of Immediate Implants With or Without a Volume-stable Collagen Matrix: a Randomized Controlled Clinical Trial
University of Pisa
40 participants
Nov 1, 2021
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to evaluate the soft tissue clinical results in patients that received, or not, a soft tissue augmentation around dental implant inserted immediately after the extraction.
Eligibility
Inclusion Criteria1
- \- Presence of a single failing tooth in the esthetic region (second premolar to contralateral second premolar), the adjacent teeth should be present and without any dental pathologies.
Exclusion Criteria9
- Patients who are heavy smokers (more than 10 cigarettes/day);
- Patients who suffer from any systemic diseases that could negatively influence wound healing;
- Patients who received head and neck radiation treatment;
- Patients who have a full contraindication to implant surgery;
- Patients who have uncontrolled periodontal disease;
- Patients who show a full mouth plaque and bleeding score higher than 25%;
- Patients who have deficient extraction sockets according to the classification of Juodzbalys et al. 2008.
- Patients with known allergy, sensitivity or intolerance to collagen
- Patients who are pregnant or who are breastfeeding
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Interventions
After tooth extraction and implant insertion the Test group will receive a soft tissue augmentation on the buccal side oh the implant. an envelop flap will be raised and a volume-stable collagen graft will be stabilized with sutures. Control group will not receive soft tissue augmentation.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05081284