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This study investigates the long-term performance of the Socket Shield Technique (SST) for preserving the bone and soft tissue around dental implants when used with two different timing protocols: immediate versus delayed implant placement.
SST is a surgical technique where a thin portion of the tooth root (the buccal shield) is intentionally retained to support the facial bone and gum tissues after tooth extraction. While SST is known to enhance esthetics and preserve bone in the short term, little evidence exists on its long-term effectiveness in different clinical scenarios.
This randomized clinical trial enrolled patients who needed single-tooth implants in the esthetic zone. Participants were randomly assigned to one of two groups:
Immediate SST group: the implant was placed at the same time the socket shield was prepared.
Delayed SST group: implant placement was performed six months after socket shield preparation.
Over a 6-year follow-up period, both groups were evaluated for:
Changes in ridge width and bone height using CBCT imaging. Esthetic outcomes using the Pink Esthetic Score (PES). Patient satisfaction through a structured questionnaire.
The goal is to determine whether SST offers reliable long-term outcomes in either immediate or delayed implant placement scenarios, supporting its broader clinical use.
This randomized controlled clinical trial was conducted to compare the long-term clinical, radiographic, esthetic, and patient-reported outcomes of the SST when used with either immediate or delayed implant placement in the anterior maxilla.
Study Design:
Parallel-arm, randomized controlled trial Conducted at the Faculty of Dentistry, Mansoura University Sample: 25 patients needing single-tooth replacement
Groups:
Immediate SST: implant placed at time of shield preparation Delayed SST: implant placed after 6-month healing
Primary Outcome:
Ridge Width Change: measured at 1 mm, 2 mm, 4 mm, and 6 mm apical to the implant platform using standardized CBCT imaging at baseline, 1 year, and 6 years.
Secondary Outcomes:
Buccal/Palatal Bone Height Implant Stability Pink Esthetic Score Patient Satisfaction
Serial CBCT scans were superimposed using the Fusion module of OnDemand3D software for precise assessment. All clinical assessments were performed by calibrated, blinded examiners. Statistical analysis was performed using SPSS, with significance set at p < 0.05.
This study provides one of the first long-term comparative evaluations of SST in different implant placement protocols, offering evidence to support its clinical reliability over a 6-year period.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Immediate Implant Placement with SST | Active Comparator | Participants received the SST with immediate implant placement performed at the time of extraction. |
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| Delayed Implant Placement with SST | Active Comparator | Participants received the SST with delayed implant placement, performed 6 months after extraction and shield preparation. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Immediate Implant Placement with SST | Procedure | Participants underwent extraction and socket shield preparation, followed by immediate implant placement in the esthetic maxillary zone. The implant was inserted at the same surgical session using a flapless or minimally invasive approach. CBCT was used to guide planning and assess ridge dimensions. Healing and follow-up assessments were conducted at 1 year and 6 years post-placement. |
| Measure | Description | Time Frame |
|---|---|---|
| Horizontal Ridge Width Change at 1, 2, 4, and 6 mm Apical to the Implant Platform | Ridge width was measured at 1 mm, 2 mm, 4 mm, and 6 mm apical to the implant platform using standardized CBCT scans. Superimposed scans were aligned using the Fusion module of OnDemand3D™ software. Changes in horizontal ridge width were calculated by subtracting baseline values from those at 1 year and 6 years to assess dimensional stability over time. Unit of Measure: → Millimeters (mm) Safety Issue: → No | Immediately after implant placement (baseline), 1 year, and 6 years post-placement |
| Measure | Description | Time Frame |
|---|---|---|
| Buccal and Palatal Bone Height Change | Bone height was measured from the implant apex to the most coronal point of the buccal and palatal bone crest using CBCT. Changes were calculated at each follow-up relative to baseline. Unit of Measure: → Millimeters (mm) Safety Issue: → No | Immediately after implant placement (baseline), 1 year, and 6 years post-placement |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Soaad Tolba Badawy, Lecturer, Oral Surgery, MU | Faculty of dentistry, Mansoura university | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Faculty of Dentistry, Mansoura University | Al Mansurah | Dakahlia Governorate | 35511 | Egypt |
The individual participant data will not be shared due to privacy considerations, and limitations in participant consent regarding external data sharing.
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Participants were randomized into two parallel groups: one receiving immediate implant placement and the other delayed placement following the SST. Each group followed the assigned intervention protocol throughout the study.
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The radiographic outcomes assessor was blinded to group allocation. No other masking was implemented due to the surgical nature of the intervention.
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| Delayed Implant Placement with SST | Procedure | Participants underwent extraction and socket shield preparation. Implant placement was delayed for 6 months to allow soft and hard tissue healing. The implant was placed after verifying shield stability and ridge preservation via CBCT. Follow-up assessments were conducted at 1 year and 6 years post-placement. |
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| Implant Stability Quotient (ISQ) | Implant stability was assessed using a resonance frequency analysis device (Osstell ISQ). Buccolingual and mesiodistal values were averaged to calculate ISQ. Unit of Measure: → ISQ Units Safety Issue: → No | Immediately after implant placement, loading time and 1-year post-placement |
| Pink Esthetic Score (PES) | The esthetic outcome was assessed using the PES, evaluating five parameters each scored from 0-2. Total PES ranges from 0-10, with ≥6 considered clinically acceptable. Unit of Measure: → Score (0-10) Safety Issue: → No | At implant loading, 1 year, and 6 years post-placement |
| Patient Satisfaction (VAS Score) | Satisfaction was measured using a 100 mm visual analog scale (VAS) on three dimensions: overall experience, expectations, and esthetics. Scores were converted into percentages. Unit of Measure: → VAS (%) Safety Issue: → No | At implant loading, 1 year, and 6 years post-placement |