NCT05081284

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

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (estimated)
• Sponsor: University of Pisa · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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.

Detailed description

After being informed about the study and potential risks, all patients giving written informed consent will undergo a screening period to determinate eligibility for study entry. Patients who meet eligibility requirements will be randomized in this single blinded(investigator) study. Group (Test) will receive immediate implant after extraction and a soft tissue augmentation with a collagen matrix. Group (Control) will receive only immediate implant after extraction without soft tissue augmentation.

Conditions

• Edentulous Alveolar Ridge

Interventions

Type	Name	Description
DEVICE	Volume-stable collagen matrix Geistlich Fibro-Gide®	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.

Timeline

• Start date: 2021-11-01
• Primary completion: 2024-11-01
• Completion: 2025-11-01
• First posted: 2021-10-18
• Last updated: 2024-05-09

Locations

1 site across 1 country: Italy