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Comparison of Split Box and Split Bone Block Techniques in Horizontal Ridge Augmentation (SBBTvsSBT)

16 giugno 2026 aggiornato da: Marmara University

Comparison of Radiological Bone Gain and Resorption Between the Split Box Technique and the Split Bone Block Technique, and Evaluation of Implant Survival: a Retrospective Study

Horizontal alveolar ridge deficiencies may prevent the placement of dental implants and often require bone augmentation procedures before implant treatment. Two techniques commonly used for horizontal ridge augmentation are the Split Box Technique and the Split Bone Block Technique.

This retrospective study included patients treated at Marmara University Faculty of Dentistry between January 2014 and January 2026. Radiographic records were reviewed to evaluate bone gain after augmentation and the stability of the augmented bone during long-term follow-up. Implant survival after prosthetic rehabilitation was also assessed.

The purpose of this study was to compare the long-term outcomes of the Split Box Technique and the Split Bone Block Technique in terms of bone gain, bone stability, and implant survival.

Panoramica dello studio

Descrizione dettagliata

Horizontal alveolar ridge deficiencies often require augmentation procedures before dental implant placement. Among the available augmentation methods, the Split Bone Block Technique (SBBT) and the Split Box Technique (SBT) are autogenous bone augmentation approaches designed to increase horizontal ridge width and facilitate implant-supported rehabilitation.

The aim of this retrospective study was to compare the radiological outcomes of SBBT and SBT with respect to horizontal bone gain, long-term bone stability, and implant survival. In addition, postoperative complications associated with both techniques were evaluated.

Patients treated between January 2014 and January 2026 at the Department of Oral and Maxillofacial Surgery, Marmara University Faculty of Dentistry, were retrospectively screened. Patients who underwent horizontal ridge augmentation using either SBBT or SBT and had complete radiographic follow-up records were included in the study.

Cone-beam computed tomography (CBCT) images obtained preoperatively, 6 months after augmentation, and during long-term follow-up after prosthetic rehabilitation were used to assess changes in horizontal bone width and graft stability. Radiological measurements were performed to evaluate bone gain after augmentation, dimensional changes during follow-up, and long-term maintenance of the augmented ridge.

The primary outcome measures were horizontal bone gain and long-term bone resorption. Secondary outcome measures included implant survival following definitive prosthetic rehabilitation and the occurrence of postoperative complications.

The study was designed to determine whether the Split Box Technique and the Split Bone Block Technique provide comparable long-term clinical and radiological outcomes for the treatment of horizontal alveolar ridge deficiencies prior to implant placement.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

31

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Istanbul
      • Istanbul, Istanbul, Turchia (Türkiye), 34854
        • Marmara University Faculty of Dentistry, Department of Oral and Maxillofacial Surgery

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

The study population consisted of adult patients with horizontal alveolar ridge deficiencies who underwent horizontal ridge augmentation using either the Split Box Technique or the Split Bone Block Technique before implant placement. Patients were treated at Marmara University Faculty of Dentistry between January 2014 and January 2026 and had complete clinical records and CBCT imaging available for retrospective evaluation.

Descrizione

Inclusion Criteria:

  • Age ≥18 years.
  • Patients with horizontal alveolar ridge deficiency requiring horizontal ridge augmentation before implant placement.
  • Patients treated with either the Split Box Technique (SBT) or Split Bone Block Technique (SBBT) at Marmara University Faculty of Dentistry between January 2014 and January 2026.
  • Availability of complete radiographic records, including CBCT scans obtained preoperatively (T0), 6 months after augmentation (T1), and during long-term follow-up after prosthetic loading (T2).
  • Availability of complete clinical records and follow-up data.

Exclusion Criteria:

  • Incomplete clinical or radiographic records.
  • Patients lost to follow-up.
  • Presence of uncontrolled systemic diseases or conditions known to adversely affect bone healing.
  • Use of medications known to interfere with bone metabolism or healing.
  • Active infection at the augmentation site or complications that altered the planned treatment protocol.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Split Bone Block Technique (SBBT)
Patients who underwent horizontal alveolar ridge augmentation using the Split Bone Block Technique.
Autogenous horizontal ridge augmentation procedure using cortical bone plates harvested from the mandibular ramus to reconstruct deficient alveolar ridges prior to implant placement.
Altri nomi:
  • SBBT
Split Box Technique (SBT)
Patients who underwent horizontal alveolar ridge augmentation using the Split Box Technique.
Autogenous horizontal ridge augmentation procedure involving mobilization and fixation of a buccal bone segment to increase horizontal ridge width prior to implant placement.
Altri nomi:
  • SBT

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Long-Term Horizontal Bone Gain
Lasso di tempo: From baseline (preoperative CBCT) to long-term follow-up after prosthetic loading(average follow-up: 4.2 years)
Overall change in horizontal alveolar ridge width from baseline to long-term follow-up after prosthetic loading, measured on CBCT images.
From baseline (preoperative CBCT) to long-term follow-up after prosthetic loading(average follow-up: 4.2 years)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Implant Survival Rate
Lasso di tempo: From implant placement through study completion (average follow-up: 4.2 years)
Survival of dental implants placed in augmented sites following prosthetic rehabilitation.
From implant placement through study completion (average follow-up: 4.2 years)
Postoperative Complications
Lasso di tempo: From augmentation surgery through study completion (average follow-up: 4.2 years)
Occurrence of complications related to augmentation procedures, including wound dehiscence, infection, graft exposure, and neurosensory disturbances.
From augmentation surgery through study completion (average follow-up: 4.2 years)
Long-Term Bone Resorption
Lasso di tempo: From 6 months after augmentation surgery to long-term follow-up after prosthetic loading (average follow-up: 4.2 years)
Change in horizontal ridge width between the post-augmentation healing period and long-term follow-up, measured on CBCT images.
From 6 months after augmentation surgery to long-term follow-up after prosthetic loading (average follow-up: 4.2 years)
Horizontal Bone Gain
Lasso di tempo: From baseline (preoperative CBCT) to 6 months after augmentation surgery
Change in horizontal alveolar ridge width from baseline to 6 months after augmentation, measured on CBCT images.
From baseline (preoperative CBCT) to 6 months after augmentation surgery

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Guhan Dergin, DDS, PhD, Marmara University Faculty of Dentistry

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 gennaio 2014

Completamento primario (Effettivo)

1 gennaio 2026

Completamento dello studio (Effettivo)

1 gennaio 2026

Date di iscrizione allo studio

Primo inviato

5 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

16 giugno 2026

Primo Inserito (Effettivo)

18 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

18 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2025-11-02/2025-86 (Altro identificatore: Marmara University Faculty of Dentistry Clinical Research Ethics Committee Approval)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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