About this trial
The aim of this research project is to compare two surgical procedures to improve soft tissue volume. Both procedures have already been validated, but despite their great clinical relevance, little data exists in the literature. With this study, the investigators aim to evaluate volumetric changes of connective tissue graft versus biomaterial (membrane). In addition, further clinical measurements will be taken and patient satisfaction will be assessed.
Eligibility criteria
Qualifiers
Informed Consent signed by the subject
Age ≥ 18 years
Willingness to sign informed consent and to participate in the study
Single tooth gap or extended edentulous space in the lower or posterior jaw including a pontic site with a soft tissue deficiency.
Disqualifiers
Any physical or mental disorder that would interfere with the ability to perform adequate oral hygiene or the capability of providing written informed consent and compliance with the protocol
Severe bruxism, clenching habits, or presence of oro-facial pain
Uncontrolled diabetes mellitus (HbA1c >7.0)
Clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, etc.)
Trial design
Treatments tested in this trial
- Geistlich Fibro-Gide®