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NCT05729607
Vertical Soft Tissue Augmentation With CTG vs ADM
Conditions: Implant Complication
Sex: All
Ages: 18 Years – 99 Years
Healthy volunteers: 1
Phase: NA
Enrollment: 28
Sponsor: Harvard Medical School (HMS and HSDM)
Location: United States
Summary
The study aims at comparing two different approaches for vertical soft tissue augmentation at implant sites exhibiting soft tissue dehiscences: autogenous connective tissue graft vs acellular dermal matrix + enamel matrix derivative
Eligibility Criteria
Inclusion criteria:Age ≥ 18 yearsPeriodontally and systemically healthyFull-mouth plaque score and full-mouth bleeding score ≤ 20% (measured at four sites per tooth)Presence of single functional dental implant in the anterior with a PSTDImplants diagnosed as healthy (Berglundh et al., 2018)Exclusion criteria are:Contraindications for surgerySystemic condition (e.g.
diabetes mellitus, HIV, cancer, etc) that could compromise wound healingPatients pregnant or attempting to get pregnant (self-reported)Untreated periodontitisUntreated peri-implant mucositis or peri-implantitis (Berglundh et al., 2018)Smoking, defined as self-reported daily habit.
Occasional smokers won't be excludedHistory of soft tissue grafting at the implant site within the last 6 months
Source: ClinicalTrials.gov (NCT05729607). StuddyBuddy aggregates publicly available trial information.