About this trial
The study suggests that if the investigators used customized healing abutments synthesized from PEEK may have a favorable effect on peri-implant soft tissues regarding decreased plaque accumulation and healing stimulation compared to the customized conventional titanium healing abutments.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients should be systematically free from any disease as according to Cornell Medical Index-Health Questionnaire .
Both genders.
Age from 20-50 years.
Missing tooth in esthetic zone (Anterior/Premolar) to be restored with standard implant, with no need for additional bone and soft tissue augmentation procedures.
Disqualifiers
Poor oral hygiene condition.
Pregnant and lactating females.
Smokers.
Trial design
Parallel
Treatments tested in this trial
PEEK customized healing abutment
DeviceGuided delayed implant and a customized PEEK healing abutment placed simultaneously with implant surgery
Titanium customized healing abutment
DeviceGuided delayed implant and a customized Titanium healing abutment placed simultaneously with implant surgery
Treatment groups
Trial outcomes
Primary outcomes
Clinical evaluation of peri-implant soft tissue changes
Clinical evaluation of peri-implant soft tissue changes the Probing Depth (PD).
Clinical evaluation of peri-implant soft tissue changes
Clinical evaluation of peri-implant soft tissue changes the Plaque Index (PI) score.
Clinical evaluation of peri-implant soft tissue changes
Clinical evaluation of peri-implant soft tissue changes the Gingival Index (GI)score.
Clinical evaluation of peri-implant soft tissue changes
Clinical evaluation of peri-implant soft tissue changes the Gingival Bleeding Time Index (GBTI).
Secondary outcomes
Biochemical evaluation
Biochemical evaluation of peri-implant sulcus fluid (PISF) total bacterial load.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.