The goal of this clinical trial is to evaluate effect of customized healing abutment in patients who need single implant reconstruction. The main question it aims to answer is: • effect of customized healing abutment on peri-implant soft and hard tissue Participants will received customized healing abutments before final prostheses delivery.
Patients who need single implant restoration will be received one- stage implant placement with utilization of customized healing abutment. Data collection about change in hard and soft tissue will be collected digitally at several times points. Patients will received single crown on implant as final prosthesis. Change in peri-implant tissue will be analyzed with digital softwares.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
patients will undergoes one-stage implant placement with customized healing abutments with different macrogeometry and emergence angle made prior to the surgery and will be inserted without sutures, after osseointegration completed patients will received single crown on implant.
patients will undergoes one-stage implant placement with standard titanium healing abutment made prior to the surgery and will be inserted without sutures, after osseointegration completed patients will received single crown on implant.
Department of Prosthodontics, Faculty of Dentistry, Chiang Mai University
Chiang Mai, Thailand
soft tissue alteration
peri-implant soft tissue change compared to baseline including vertical and horizontal soft tissue alteration by superimposing intraoral scan at different time points
Time frame: T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up
hard tissue alteration
peri-implant marginal bone change compared to baseline at different time points by periapical radiograph
Time frame: T0 baseline before implant placement, 6month follow up, 12month follow up
volumetric alteration
peri-implant volumetric change at different time points compared to baseline with superimposing intraoral scan
Time frame: T0 baseline before implant placement,T1 1month follow up, 4month follow up, 6month follow up, 12month follow up
pain numerical rating scale
pain assessment at time of final prosthesis delivery with scale from 0 to 10
Time frame: at prosthesis delivery, 2 hours and 24 hours after prosthesis delivery
pink esthetic score
pink esthetic score change compared to before implant treatment
Time frame: T0 baseline before implant placement, 6 month follow up
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