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

2026년 6월 16일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

관찰

등록 (실제)

31

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

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.

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
개입 / 치료
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.
다른 이름들:
  • 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.
다른 이름들:
  • SBT

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Long-Term Horizontal Bone Gain
기간: 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)

2차 결과 측정

결과 측정
측정값 설명
기간
Implant Survival Rate
기간: 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
기간: 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
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Guhan Dergin, DDS, PhD, Marmara University Faculty of Dentistry

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2014년 1월 1일

기본 완료 (실제)

2026년 1월 1일

연구 완료 (실제)

2026년 1월 1일

연구 등록 날짜

최초 제출

2026년 6월 5일

QC 기준을 충족하는 최초 제출

2026년 6월 16일

처음 게시됨 (실제)

2026년 6월 18일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 16일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

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

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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