Partial edentulism
Conditions
Interventions
Experimental group:Ultra-Smooth Abutments
Control group:Conventional Abutments
Sponsors
Hospital of Stomatology, SunYat-sen University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1.Aged over 18 and under 75 years old, no gender restriction; 2.Patients with partial edentulism requiring implant-supported prostheses; 3.Participants who are willing and able to provide written informed consent, adhere to the study protocol, and attend scheduled follow-up visits.
Exclusion criteria
Exclusion criteria: 1.Patients with local or systemic diseases that preclude tolerance to implant surgery, or conditions compromising osseointegration of implants, including uncontrolled diabetes mellitus (glycated hemoglobin > 7%), severe cardiovascular diseases (e.g., unstable angina, uncontrolled hypertension), uncontrolled hyperthyroidism or hypothyroidism, hematological disorders, long-term use of medications interfering with bone metabolism, and a history of local radiotherapy; 2.Heavy smoking, defined as >=10 cigarettes per day; 3.Pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Peri-implant buccal soft tissue recession; | — |
Secondary
| Measure | Time frame |
|---|---|
| Marginal bone level (MBL) change;soft tissue Pink Esthetic Score (PES);Changes in papilla position;Bleeding Index (BI);modified Plaque Index (mPI);probe depth (PD);Implant survival rate; | — |
Countries
China
Contacts
Public ContactYu Xiaolin
Hospital of Stomatology, SunYat-sen University
Outcome results
None listed