Clinical application of fully digital processes in immediate full-arch implant restoration

INTERVENTION: Control Group:Conventional workflow;Experimental Group:Digital workflow; CONDITION: Edentulism or Terminal Dentition PRIMARY OUTCOME: Immediate prosthesis delivery time;Occlusal adjustment amount of prosthesis; SECONDARY OUTCOME: Prosthesis survival rate;Incidence of prosthetic complications;Prosthesis seating condition;Implant survival rate;Patient‐reported outcomePatient‐reported outcome (oral health‐related quality of life); INCLUSION CRITERIA: 1. Age 18 or older, any gender; 2. Patients with a single jaw at the end of the dentition or who are edentulous, and need full‐arch implant immediate restoration; 3. Able to achieve good initial stability during implant surgery (e.g., insertion torque =35 N·cm or clinically assessed as able to bear immediate load); 4. Overall good health with no contraindications for implant surgery; 5. Good oral hygiene and able to cooperate with treatment and follow‐up; 6. Voluntarily willing to participate in this study and sign the informed consent form.