Acellular Dermal Matrix, Dental Implant, Immediate Dental Implant Placement, Polytetrafluoroethylene, Soft Tissue Augmentation at Dental Implants
Conditions
Keywords
Acellular Dermal Matrix, Immediate Dental Implants, Soft-tissue augmentation, Tissue Phenotype, d-PTFE
Brief summary
To evaluate soft tissue augmentation using acellular dermal matrix (ADM) over immediately placed dental implants in anterior maxilla.
Detailed description
This randomized clinical trial was designed to evaluate and compare the efficacy of ADM versus d-PTFE membranes in the preservation of the peri-implant hard and soft tissues in the setting of immediate implant placement on the anterior maxilla.
Interventions
The socket with immediately placed dental implant was covered with a d-PTFE membrane cut to fit the surgical site
The socket with immediately placed dental implant was covered with ADM that was inserted into facial and palatal split thickness pouches.
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with non-restorable maxillary anterior tooth/teeth. * Good oral hygiene. * Patients' cooperation and fully capable to comply with the study protocol. * Age ranges from 18 to 45 years. * Free from history of parafunctional habits e.g. clenching and bruxism * Sufficient inter- arch space.
Exclusion criteria
* Any local pathological condition that contraindicates implant placement. * Pregnancy. * Medication that affects bone healing. * Psychological problems. * Patient had undergone radiation therapy to the head and neck area in the past 12 months.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Peri-implant soft-tissue phenotype | Six months following implant placement | A standardized periodontal probe was used to clinically measure the keratinized mucosal width, supracrestal tissue height, and mucosal thickness. They were measured in millimeters (mm) |
Countries
Egypt