This retrospective study was conducted in accordance with the Declaration of Helsinki. The study protocol was approved by the Ethics Committee of WuYi County Stomatological Hospital (Approval No. 2025-1) on February 25, 2025. Patients treated between January 2020 and December 2022 were enrolled. Written informed consent was obtained from all participants for study participation and publication of de-identified clinical images. The research tools used in this experiment are listed in the Table of Materials. The study workflow is illustrated in Figure 1.

Figure 1: Study workflow. Flowchart illustrating patient enrollment, group allocation, restorative procedures, and follow-up evaluations performed at 3 months and 2 years after restoration. Please click here to view a larger version of this figure.
1. Study design
This retrospective study enrolled patients treated between January 2020 and December 2022 who met the predefined eligibility criteria.
- Inclusion criteria
Patients were eligible for inclusion if they met all of the following criteria: posterior tooth defects confirmed by dental radiographs, with root canal treatment completed more than 1 week previously; radiographs demonstrating adequate root canal filling, no significant periapical radiolucency, no alveolar bone resorption, and healthy periodontal tissues; absence of percussion pain or tooth mobility; sufficient remaining tooth structure to support either all-ceramic onlay or fiber post-and-core crown restoration; normal posterior occlusion without parafunctional habits such as bruxism or clenching; no acute or severe systemic disease that would contraindicate treatment; and normal cognitive function with the ability to cooperate throughout treatment.
- Exclusion criteria
Patients were excluded if they presented with uncontrolled residual pulpitis, apical periodontitis, temporomandibular joint disorder syndrome, poor oral hygiene, active periodontitis, absence of an opposing tooth, presence of a removable prosthesis as the opposing dentition, abnormal occlusal habits, pregnancy or lactation, anatomical abnormalities such as malformed teeth, or temporomandibular joint disease.
2. Fiber post-and-core crown restoration treatment
The fiber post-and-core crown restoration procedure was performed according to a standardized protocol. Tooth shade was determined within 5 s under natural light using a shade guide to minimize visual fatigue. Based on the working length established during root canal treatment and the root diameter observed on dental radiographs, the post space was sequentially prepared with P-drills and then shaped with a fiber post-shaping drill. The post diameter was maintained at approximately one-quarter to one-third of the root diameter. The post length was planned to be at least equal to the clinical crown length, with the intrabony portion extending beyond one-half of the root length within the alveolar bone while preserving a minimum 5 mm apical seal. The root canal walls were confirmed to be smooth before post placement.
A glass fiber post of appropriate length and diameter was selected and tried in to confirm an accurate fit. The post was immersed in 75% alcohol, shaken, and air-dried. The root canal was irrigated with saline, ultrasonically cleaned, disinfected with 75% alcohol, and dried. A self-etch adhesive was applied to both the root canal walls and the post surface, then light-cured for 15 s. Dual-cure resin cement was injected from the base of the post space, the post was inserted, and the assembly was light-cured for 40 s. A resin core was subsequently built up using core resin and light-cured.
Tooth preparation was performed according to the requirements for an all-ceramic crown, including a uniform 1.0 mm occlusal reduction, elimination of undercuts on all surfaces, and a chamfer finish line at the cervical margin. Impressions were obtained using a two-step addition silicone technique. Following gingival displacement with retraction cords, a heavy-body impression was made, followed by a light-body wash impression using the double-cord technique. A temporary crown was fabricated and cemented to protect the prepared tooth and maintain the prepared space until definitive restoration.
The tooth shade was reconfirmed, and a super-hard plaster model was prepared. The occlusal relationship was recorded using bite registration silicone and submitted to the dental laboratory for fabrication of a zirconia full crown. During the clinical try-in, proximal contacts and marginal adaptation were evaluated using articulating paper (40 µm and 200 µm) and adjusted as necessary.
For final bonding, the intaglio surface of the crown and the prepared tooth were cleaned and dried. Dual-cure resin cement was mixed and applied to the internal surface of the restoration. The crown was fully seated, and excess cement was tack-cured for 1–2 s before removal. Final light curing was then performed from multiple directions for 20 s per surface. Iodine glycerin was applied to the gingival sulcus, and patients were instructed to avoid chewing hard foods on the treated side for 24 h (Figure 2).

Figure 2: Representative clinical images of posterior tooth restoration with a fiber post-and-core crown. (A) Clinical appearance of the tooth 1 week after root canal treatment, before restoration. (B) Placement of the fiber post within the prepared root canal. (C) Bonding and core build-up following fiber post placement. (D) Immediate postoperative appearance after placement of the definitive crown. Please click here to view a larger version of this figure.
3. All-ceramic onlay restoration
The all-ceramic onlay restoration procedure was performed according to a standardized protocol. Tooth shade was determined within 5 s under natural light using the same shade guide described for the fiber post-and-core crown group. Discolored, softened, and structurally weakened cusp tissue was removed. A P-drill was used to remove 1–2 mm of gutta-percha from the root canal orifice, after which the canal was irrigated with saline, dried, disinfected with 75% alcohol, and treated with a self-etch adhesive. The canal orifice was sealed with flowable resin and light-cured for 40 s. The cavity was prepared with a flat pulpal floor, straight axial walls, and no undercuts. Occlusal reduction consisted of 1.5 mm on functional cusps and 1.0 mm on non-functional cusps while maintaining a remaining tooth thickness greater than 3 mm. The cavity walls were flared at approximately 6°, with rounded internal line angles, a convergence angle of 2°–6°, and a 90° shoulder finish line.
Impressions were obtained using the same two-step addition silicone technique described for the fiber post-and-core crown group. A temporary onlay was fabricated and placed to protect the prepared tooth. The occlusal relationship was recorded using bite registration silicone, and the working model was submitted to the dental laboratory for fabrication of a lithium disilicate ceramic onlay. During the clinical try-in, marginal adaptation was evaluated using a periodontal probe, interproximal contacts were assessed using dental floss, and the shape and shade of the restoration were confirmed with the patient.
For final bonding, the intaglio surface of the onlay was etched with 9.5% hydrofluoric acid for 40 s, rinsed thoroughly, neutralized with sodium bicarbonate, ultrasonically cleaned in 95% alcohol for 5 min, and dried. A silane coupling agent followed by an adhesive was applied to the restoration surface. The prepared tooth was isolated, etched with 35% phosphoric acid for 30 s, rinsed, and dried. Adhesive was applied and light-cured for 15 s. The onlay was bonded using dual-cure resin cement, excess cement was removed, and the restoration was light-cured for 40 s. Occlusion was adjusted as required, and the restoration was polished (Figure 3).

Figure 3: Representative clinical images of posterior tooth restoration with an all-ceramic onlay. (A) Clinical appearance of the tooth 1 week after root canal treatment, before restoration. (B) Tooth preparation for the all-ceramic onlay. (C) Lithium disilicate ceramic onlay before placement. (D) Immediate postoperative appearance after onlay try-in and definitive bonding. Please click here to view a larger version of this figure.
4. Operator standardization and calibration
To minimize operator-related variability, all restorative procedures were performed by three prosthodontists who followed standardized clinical protocols. Before patient enrollment, all operators completed a 2-week calibration program using typodont models. A detailed operative manual was provided, and weekly review sessions were conducted to reinforce adherence to the standardized procedures. Intraoperative checklists were used to ensure consistency during critical procedural steps. All completed restorations were subsequently reviewed by a senior prosthodontist for quality assurance. In addition, quarterly inter-operator calibration sessions were conducted to review representative cases and standardize clinical decision-making. These measures were implemented to ensure procedural consistency throughout the study.
5. Clinical evaluation
Clinical outcomes were evaluated at 3 months and 2 years after restoration by two dentists with more than 15 years of clinical experience who were not involved in the treatment procedures. Both examiners were blinded to group allocation. Before the formal evaluations, the examiners completed three calibration sessions using 20 representative cases to standardize the interpretation of all evaluation indices. Inter-examiner agreement was excellent, with Cohen's κ values ranging from 0.82 to 0.91 and intraclass correlation coefficients (ICC) ranging from 0.88 to 0.94.
6. Outcome measures
- Restoration integrity
Restoration integrity was classified as follows: Grade A, the restoration was intact without defects; Grade B, the restoration exhibited minor damage that did not affect function; and Grade C, the restoration was fractured or detached.
- Tooth integrity
Tooth integrity was classified as follows: Grade A, the tooth hard tissue was intact without defects; Grade B, minor defects or cracks were present in the tooth hard tissue; and Grade C, significant hard-tissue defects were present that could potentially affect tooth function.
- Marginal adaptation
Marginal adaptation was classified as follows: Grade A, no detectable gap was present between the tooth and the restoration margin, and the periodontal probe did not catch; Grade B, a slight marginal gap was present, with slight probe catch; and Grade C, a significant marginal gap allowed insertion of the periodontal probe.
- Interproximal contacts
Interproximal contacts were classified as follows: Grade A, dental floss passed through the contact area with resistance; Grade B, dental floss passed with slight resistance and mild food impaction was present; and Grade C, dental floss passed without resistance, accompanied by severe food impaction.
- Periodontal pocket depth
Periodontal pocket depth was measured using a periodontal probe that was cleaned and disinfected before each examination. The probe was held using a modified pen grasp, and a standardized probing force of 20–25 g was applied. The probe was inserted to the base of the periodontal pocket, and the probing depth was recorded in millimeters. Greater probing depths indicated poorer periodontal outcomes.
- Gingival index
The Gingival Index was used to evaluate the severity of gingival inflammation according to gingival color, consistency, and bleeding tendency. Examinations were performed under standardized conditions using a blunt-ended periodontal probe at six sites per tooth (mesiobuccal, midbuccal, distobuccal, mesiolingual, midlingual, and distolingual). The highest score recorded for each tooth was used for analysis. Scores ranged from 0 to 3, where 0 indicated normal gingiva with no bleeding on probing; 1 indicated mild erythema and edema without bleeding on probing; 2 indicated moderate redness, edema, a shiny appearance, and bleeding on probing; and 3 indicated severe redness, swelling, spontaneous bleeding, or ulceration. Higher scores indicated poorer periodontal health.
- Plaque index
The Plaque Index was used to evaluate the thickness and amount of plaque accumulation at the gingival margin of the index teeth. Examinations were performed by visual inspection combined with gentle probing of the tooth surface. Each tooth was scored from 0 to 3 according to the following criteria: 0, no plaque at the gingival margin; 1, a thin plaque film adherent to the gingival margin that was not visible to the naked eye but detectable by probing; 2, moderate plaque accumulation visible at the gingival margin or on adjacent tooth surfaces; and 3, abundant soft deposits filling the gingival sulcus and covering the gingival margin and adjacent tooth surfaces. Higher scores indicated poorer oral hygiene and greater plaque accumulation.
- Chewing function
Chewing function was assessed by measuring bite force and masticatory efficiency. Bite force was measured using a bite force tester. Masticatory efficiency was determined using the sieving and weighing method and expressed as the percentage of food comminuted within a standardized chewing period. Participants were instructed to chew 5 g of peanuts for 20 s before expectorating all chewed material into a collection container. The oral cavity was then rinsed to recover any remaining food particles. The collected material was passed through a 2.0 mm sieve, and the residue retained on the sieve was dried and weighed. Masticatory efficiency was calculated as:
(total weight - residual weight)/total weight × 100%.
- Oral health-related quality of life
Oral health-related quality of life was evaluated using the Chinese version of the Oral Health Impact Profile-14 (OHIP-14), a validated instrument widely used to assess the psychosocial impact of oral conditions on daily life. The questionnaire comprises 14 items across seven domains: functional limitation, physical pain, psychological discomfort, physical disability, psychological disability, social disability, and handicap. Each item is scored on a 5-point Likert scale ranging from 0 ("never") to 4 ("very often"), yielding a total score of 0–56, with higher scores indicating poorer oral health-related quality of life. The Chinese version of the OHIP-14 has demonstrated good reliability and validity (Cronbach's α = 0.93)15, supporting its use for evaluating oral health outcomes in Chinese populations.
7. Statistical analysis
Statistical analyses were performed using SPSS software. Normally distributed continuous variables were expressed as mean ± standard deviation and compared using the independent-samples t-test. Non-normally distributed continuous variables were expressed as median (Q1, Q3) [M (Q1, Q3)] and compared using the Mann-Whitney U test. Categorical variables were expressed as numbers (percentages) and compared using the χ2 test, continuity-corrected χ2 test, or Fisher's exact test, as appropriate. Ordinal variables were compared using the Mann-Whitney U test. All statistical tests were two-sided, and P < 0.05 was considered statistically significant.