Evaluation the Accuracy of Immediate Implant Placement Using SocketFit Static Surgical Guide Versus Conventional Static Surgical Guide in Anterior Esthetic Zone (SocketFit)
2026년 8월 11일 업데이트: Aliaa Saeed Kishk, Tanta University
This study compares two types of surgical guides used during immediate dental implant placement in the upper front teeth.
One guide is a conventional static surgical guide, while the other is a modified SocketFit static surgical guide designed to improve stability after tooth extraction.
The purpose of the study is to determine whether the SocketFit guide improves the accuracy of implant placement.The findings may help improve the precision and predictability of immediate dental implant treatment in the anterior esthetic zone.
연구 개요
상태
모병
상세 설명
Immediate implant placement in the anterior esthetic zone is a predictable treatment option that reduces treatment time and preserves peri-implant soft and hard tissues.
Static computer-guided surgery has improved the accuracy of implant placement; however, guide stability may be compromised immediately after tooth extraction because of complex morphology and angulation of post-extraction sockets, as well as variations in bone density.These factors can lead to surgical drill displacement, causing the implant to deviate from its intended trajectory.Therefore, The SocketFit static surgical guide incorporates a socket-engaging extension designed to enhance guide seating and stability during osteotomy preparation.
Limited evidence is available regarding the accuracy of this modified guide compared with the conventional tooth-supported static surgical guide.
Therefore, this study aims to evaluate the accuracy of immediate implant placement using the SocketFit static surgical guide versus the conventional static surgical guide in the anterior esthetic zone.
Accuracy will be assessed by comparing the planned and actual implant positions using postoperative Cone Beam Computed Tomography (CBCT) superimposition, evaluating coronal, apical, angular, and depth deviations.
연구 유형
중재적
등록 (추정된)
26
단계
- 해당 없음
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: Aliaa s. Kishk, Batchelor
- 전화번호: +201015101949
- 이메일: Aliaa8271staff@dent.tanta.edu.eg
연구 연락처 백업
- 이름: rehab f ghouraba, PHD
- 전화번호: +201211512429
- 이메일: rehab_ghouraba@dent.tanta.edu.eg
연구 장소
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Gharbia Governorate
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Tanta, Gharbia Governorate, 이집트, 31773
- 모병
- Periodontology Clinic at Faculty of Dentistry Tanta University
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연락하다:
- rehab f ghouraba, PHD
- 전화번호: +201211512429
- 이메일: rehab_ghouraba@dent.tanta.edu.eg
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연락하다:
- Aliaa S Kishk, Batchelor
- 전화번호: +201015101949
- 이메일: Aliaa8271staff@dent.tanta.edu.eg
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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
건강한 자원 봉사자를 받아들입니다
아니
설명
Inclusion Criteria:
- Patients in good health with absence of any relevant medical condition that contraindicates dental implant placement e.g. blood coagulation disorder.
- Optimal compliance is evidenced by no missed treatment appointments and a positive attitude toward oral hygiene.
- Extraction socket type I according to Ellian et al criteria with adequate native/apical bone to achieve primary implant stability and intact buccal plate of bone.
- Thick mucosal phenotype.
- Probing depth ≤ 3 mm at mid-buccal aspect of failing tooth.
- Age ranged from 18- 35 years old of both genders.
Exclusion Criteria:
- Patients subjected to irradiation in the head and neck area.
- Bisphosphonate therapy.
- Females who are pregnant or trying to conceive, and nursing mothers.
- Smokers and uncontrolled diabetic patients.
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: SocketFit Static Surgical Guide
Participants will undergo immediate implant placement in the anterior esthetic zone using the SocketFit static surgical guide.
The guide incorporates a socket-engaging extension designed to enhance guide stability and drilling accuracy following atraumatic tooth extraction.
Implant placement will be performed according to the planned digital workflow.
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Participants will undergo immediate implant placement in the anterior esthetic zone using the SocketFit static surgical guide.
The guide incorporates a socket-engaging extension designed to enhance guide stability and drilling accuracy following atraumatic tooth extraction.
Implant placement will be performed according to the planned digital workflow.
|
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활성 비교기: Conventional Static Surgical Guide
Participants allocated to the control group will undergo immediate implant placement in the anterior esthetic zone using a conventional tooth-supported static surgical guide designed through the standard digital workflow.
Following atraumatic tooth extraction, the guide will be seated on the remaining teeth to direct sequential osteotomy preparation and implant placement according to the preoperative virtual implant plan.
All other surgical procedures, implant system, drilling protocol, and postoperative management will be identical to those used in the experimental group.
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Participants allocated to the control group will undergo immediate implant placement in the anterior esthetic zone using a conventional tooth-supported static surgical guide designed through the standard digital workflow.
Following atraumatic tooth extraction, the guide will be seated on the remaining teeth to direct sequential osteotomy preparation and implant placement according to the preoperative virtual implant plan.
All other surgical procedures, implant system, drilling protocol, and postoperative management will be identical to those used in the experimental group.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Coronal deviation
기간: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The linear distance (mm) between the planned and actual implant positions at the coronal platform, measured by digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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apical deviation
기간: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The linear distance (mm) between the planned and actual implant positions at the implant apex, measured using digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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depth(vertical) deviation
기간: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The vertical difference (mm) between the planned and actual implant positions along the implant long axis, measured using digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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angular deviation
기간: Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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The angular difference (degrees) between the long axes of the planned and actual implant positions, measured using digital superimposition of the preoperative implant plan and postoperative Cone Beam Computed Tomography (CBCT) data.
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Immediately after implant placement following digital superimposition of the planned and actual implant positions.
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공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
스폰서
수사관
- 수석 연구원: Aliaa s. Kishk, Batchelor, Tanta University
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)
2026년 8월 1일
기본 완료 (추정된)
2027년 7월 1일
연구 완료 (추정된)
2027년 7월 1일
연구 등록 날짜
최초 제출
2026년 8월 7일
QC 기준을 충족하는 최초 제출
2026년 8월 7일
처음 게시됨 (실제)
2026년 8월 12일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 8월 13일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 8월 11일
마지막으로 확인됨
2026년 8월 1일
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- 3626
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
아니요
IPD 계획 설명
No individual participant data (IPD) will be shared.
All personal identifiers, including names and any information that could identify participants, will be removed before data analysis or sharing.
De-identified Cone Beam Computed Tomography (CBCT) images, Stereolithography (STL ) models, and summary outcome data may be used in scientific publications or presentations in accordance with participant consent, ethical approval, and institutional regulations.
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. .