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Digital VS Conventional Altered Cast Technique for Mandibular Bilateral Distal Extension RPDs

2026년 5월 7일 업데이트: Kareem Mohammed Reda, Tanta University

Digital VS Conventional Altered Cast Technique for Mandibular Bilateral Distal Extension Removable Partial Denture

This study aims to compare outcomes of digitally created altered casts with conventional altered casts in mandibular bilateral distal-extension cases.

연구 개요

상세 설명

Partially dentate adults represent an increasing proportion of the population, driven by increased life expectancy and a demographic shift from total edentulism toward partial edentulism. Fabrication of removable partial dentures for distal extension edentulous ridges presents significant clinical complexity because the teeth and residual ridge possess fundamentally different degrees of displaceability. Optimum denture support re-quires recording teeth in anatomical form and the mucosa in functional form .

The altered cast impression technique , introduced by Applegate, remains one of the most widely accepted methods for achieving optimal tissue support and accurate denture base positioning relative to tooth abutments . removable partial dentures fabricated using altered cast impression technique demonstrate improved patient comfort and preservation of oral health . However, despite these advantages, debate persists regarding the clinical significance of altered cast impression technique over single-impression techniques .

Recent advances in computer-aided design and computer-aided manufacturing have transformed the removable partial dentures framework, opening new pathways in the fabrication of RPD through additive and subtractive manufacturing . Digital intraoral scanning offers advantages, including reduced dimensional error, improved efficiency, and real-time feedback on impression accuracy and extension [13-16]. However, intraoral scanning techniques are inherently mucostatic and image-based, rendering the recording of functional impression impossible, a limitation acknowledged as necessary for optimal support in distal extension removable partial dentures . Lab scanning of conventionally prepared altered casts pre-pared by traditional methods fails to eliminate inherited errors from cast separation and reassembly.

Recent studies have introduced hybrid digital workflows that combine functional registration of the edentulous ridge with mucostatic scanning of the remaining oral structures in an effort to reproduce conventional clinical procedures while improving efficiency and precision . Most investigations on digital technology in RPD have concentrated on methods for fabricating metal frameworks and evaluating their performance.

This study aims to compare outcomes of digitally created altered casts with conventional altered casts in mandibular bilateral distal-extension cases.

연구 유형

중재적

등록 (실제)

7

단계

  • 해당 없음

연락처 및 위치

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

연구 장소

      • Tanta, 이집트
        • Tanta University

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 presented with bilateral, well-formed mandibular distal extension residual ridges covered by keratinized mucosa, with a minimum thickness of 1.5-3 mm .
  • Each participant had a sound first or second premolar serving as the terminal abutment, with a crown-to-root ratio of ≥ 1:2.
  • Comprised fully or partially dentate maxillary arches, an Angle Class I molar relationship, and adequate interarch space (7-8 mm) to accommodate the prosthesis .

Exclusion Criteria:

  • The presence of systemic conditions affecting bone metabolism or healing
  • pathological conditions in the edentulous area (e.g., residual cysts, retained roots, or severe ridge re-sorption);
  • parafunctional habits such as bruxism, clenching, or tongue thrusting
  • pro-nounced anatomical undercuts in the lingual mandible or adjacent to abutment teeth that could impede denture fabrication or insertion.

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: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Digital workflow and Digital altered cast group
Digital selective tissue placement was performed within the same Exocad design project using the free-form scan-data tool, paint and pull feature to apply the principles of selective tissue pressure technique . Using free form mesh editing tools, the buccal shelf area opposing teeth 37 and 47 was identified, and controlled tissue ward displacement of the mucosal surface was simulated while monitoring the magnitude of displacement on sectional views and with digital measurement tools. Figure 2B, F The modified mandibular dataset was saved as the digitally altered cast STL (DA), which served as the basis for the digital RPD design and subsequent denture base fabrication.
The RPD design features of fully digitally fabricated RPD illustrated in Figure 2A. Digital selective tissue placement was performed within the same Exocad design project using the free-form scan-data tool, paint and pull feature to apply the principles of selective tissue pressure technique . Using free form mesh editing tools, the buccal shelf area opposing teeth 37 and 47 was identified, and controlled tissue ward displacement of the mucosal surface was simulated while monitoring the magnitude of displacement on sectional views and with digital measurement tools.
실험적: Conventional workflow and conventional altered cast group
For the CA cast technique, one of the SLM frameworks (MF2) was adapted on the stone master cast and used as a functional impression tray (Acrostone Dental Manufacturing, Cairo, Egypt) over the distal extension areas. A selec-tive pressure impression was made according to the traditional altered cast protocol, with the distal saddle areas repoured in dental stone to obtain the CA cast. This CA was then digitized using a desktop scanner (Dove Technologies, Suzhou, China) to produce the CA cast STL. Wax rims were used to verify the jaw relationship, and the maxillary cast was mounted using a facebow transfer on a semi adjustable articulator (A7 Plus, Bio-Art Equi-pamentos Odontológicos Ltda., São Carlos, SP, Brazil), while the mandibular cast was mounted in maximum intercuspation.
For the CA cast technique, one of the SLM frameworks (MF2) was adapted on the stone master cast and used as a functional impression tray (Acrostone Dental Manufacturing, Cairo, Egypt) over the distal extension areas. A selec-tive pressure impression was made according to the traditional altered cast protocol, with the distal saddle areas repoured in dental stone to obtain the CA cast. This CA was then digitized using a desktop scanner (Dove Technologies, Suzhou, China) to produce the CA cast STL. Wax rims were used to verify the jaw relationship, and the maxillary cast was mounted using a facebow transfer on a semi adjustable articulator (A7 Plus, Bio-Art Equi-pamentos Odontológicos Ltda., São Carlos, SP, Brazil), while the mandibular cast was mounted in maximum intercuspation. Semi anatomic acrylic teeth (Acrostone Dental Manufacturing, Cairo, Egypt.) were arranged, and wax try ins were evaluated intraorally in a conventional manner prior to processing.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Assessment of the condition of ridge mucosal covering of the Removable Partial Denture constructed out of digitally altered model.
기간: at 15 days, 3 months and 6 months .
at 15 days, 3 months and 6 months .

2차 결과 측정

결과 측정
기간
Denture base fit by Pressure Indicating Paste
기간: one month
one month

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

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)

2021년 5월 30일

기본 완료 (실제)

2024년 11월 30일

연구 완료 (실제)

2024년 11월 30일

연구 등록 날짜

최초 제출

2026년 5월 1일

QC 기준을 충족하는 최초 제출

2026년 5월 7일

처음 게시됨 (실제)

2026년 5월 13일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 13일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 7일

마지막으로 확인됨

2021년 5월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • R-RP-5-21-10

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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