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临床试验/NCT07533058
NCT07533058已完成不适用

The Influence of Finishing Clear Aligner Marginal Termination Design on Subgingival Periodontal Microbiota Composition During Orthodontic Treatment: A Prospective Longitudinal Split-Mouth Study.

George Emil Palade University of Medicine, Pharmacy, Sciences and Technology of Targu Mures1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年5月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
36
试验地点
1
主要终点
Periodontal Pathogen Burden Score per Dental Arch (0-7)

研究概览

简要总结

The goal of this clinical trial is to learn whether the edge design of a finishing orthodontic clear aligner at the gumline affects the bacteria living in the groove between the tooth and the gum (the gingival sulcus) in patients undergoing the finishing phase of orthodontic treatment.

The main question it aims to answer is:

- Does a supragingival aligner edge design - which covers approximately 2 mm of gum tissue - lead to higher levels of disease-associated bacteria in the gingival sulcus compared to a juxtagingival edge design that follows the gumline exactly, after 4 and 8 weeks of aligner wear?

Researchers will compare the supragingival trimming-line design to the juxtagingival festooned design to see if covering gum tissue with the aligner edge creates conditions that favor the growth of anaerobic bacteria associated with gum disease.

Participants will:

  • Wear finishing clear aligners with both designs simultaneously - one design on the upper jaw and one on the lower jaw - for 8 weeks
  • Provide fluid samples from the gum groove at 3 visits: at the start of treatment (baseline), at 4 weeks, and at 8 weeks.

Two aligner edge designs are compared: a supragingival design, which has a straight horizontal edge positioned approximately 2 mm over the gumline, covering approximately 2 mm of gum tissue with direct contact but without entering the gum groove itself, and a juxtagingival design, which follows the natural scalloped shape of the gumline exactly, terminating at the free gingival margin without covering gum tissue and without entering the groove.

The biological rationale for comparing these two designs is the following: the supragingival design, by covering 2 mm of gum tissue, creates a partially enclosed space at the entrance of the gum groove, potentially reducing the clearance of saliva and limiting oxygen access to that area. These conditions may favor the growth of anaerobic bacteria associated with gum disease. The juxtagingival design, by following the gum contour exactly at its edge, leaves the gum groove entrance more accessible to saliva and oxygen, potentially maintaining a less favorable environment for those bacteria.

Each participant receives both designs at the same time - one on the upper jaw and one on the lower jaw - and serves as their own comparison group. This within-person (split-mouth) approach eliminates differences between individuals in general health, oral hygiene habits, and saliva composition, making the comparison between the two designs more precise.

Samples are analyzed using the PeriodontScreen Real-TM real-time PCR kit (Sacace Biotechnologies Srl, Como, Italy; CE-marked in vitro diagnostic device), which detects and quantifies seven bacteria known to cause gum disease: Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, Porphyromonas endodontalis, Fusobacterium nucleatum, and Prevotella intermedia.

The main measurement is the number of these seven bacteria that exceed the clinically significant concentration threshold defined by the kit at each jaw arch and time point. A score of 0 means none of the seven bacteria exceed the threshold; a score of 7 means all seven do.

The study hypothesis is that the supragingival trimming-line design - by covering gingival tissue and partially enclosing the sulcus entrance - creates microenvironmental conditions that favor anaerobic periodontal pathogen colonization, resulting in higher pathogen burden scores compared to the juxtagingival design after 4 and 8 weeks of finishing aligner wear.

The study is conducted during the finishing phase of orthodontic treatment, when planned tooth movements are minimal (no more than 0.5 mm per tooth), so that any differences in bacterial levels can be attributed to aligner edge design rather than to tooth movement forces.

详细描述

- BACKGROUND AND RATIONALE

Clear aligner therapy is widely used in orthodontics. Two trimming-line designs are commonly employed during the finishing phase. The supragingival design uses a straight horizontal cut positioned approximately 2 mm apical to the free gingival margin: the aligner edge covers approximately 2 mm of gingival tissue with direct contact but does not penetrate the gingival sulcus. The juxtagingival festooned design uses a scalloped cut that follows the natural contour of the free gingival margin exactly, terminating at the gingival margin without covering gingival tissue and without entering the sulcus. The two designs differ fundamentally in their relationship with the gingival margin. The supragingival design creates a semi-enclosed microenvironment at the sulcus entrance: by covering 2 mm of gingival tissue, the aligner limits access of saliva and atmospheric oxygen to the sulcus entrance region. Reduced salivary clearance and decreased oxygen tension are established conditions that favor anaerobic bacterial growth in the periodontal environment. Whether 2 mm of gingival tissue coverage by the aligner edge is sufficient to produce a measurable change in sulcular oxygen tension or salivary clearance has not been directly demonstrated and constitutes the biological hypothesis under investigation. The juxtagingival design, following the gingival contour at its margin, leaves the sulcus entrance more accessible to saliva and oxygen, potentially maintaining less favorable conditions for anaerobic colonization. These microenvironmental differences have not been investigated in published studies. No prior study has examined whether trimming-line geometry affects subgingival periodontal microbiota composition in patients undergoing aligner therapy.

  • STUDY DESIGN

This is a prospective, longitudinal, within-person (split-mouth) interventional study. Each participant receives both trimming-line designs simultaneously: supragingival on one dental arch and juxtagingival festooned on the contralateral arch. The split-mouth design controls for inter-individual variation in systemic health, oral hygiene, salivary composition, and baseline microbiological status. The aligner material (CA Pro tri-layer, SCHEU-DENTAL GmbH, Iserlohn, Germany; CE-marked thermoplastic) is identical for both designs; only trimming-line geometry differs.

  • ALLOCATION RULE (NON-RANDOMIZED)

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Single (Outcomes Assessor)

盲法说明

Three roles are distinguished.

  1. Treating clinician (orthodontist, PI): assigns trimming-line designs to arches and fabricates treatment plan; not masked (allocation is inherent to treatment planning).
  2. Sample collector (general dentistry specialist and orthodontic resident, separate from the treating clinician): performs all subgingival sampling at T0, T1, and T2 and is completely blinded to arch allocation --- the collector does not know which trimming-line design is assigned to which arch at any time point.
  3. Laboratory personnel (UMFST Microbiology and Mures County Clinical Hospital): receive coded tubes labeled with participant code, arch, and time point only, without reference to trimming-line design assignment; fully blinded to allocation. Participant awareness of their aligner design does not influence the microbiological outcome and is not considered a source of bias for this study.

入排标准

年龄范围
15 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Permanent dentition (excluding third molars)
  • •Age 15 years or older at enrollment
  • •Currently undergoing the finishing phase of orthodontic treatment with clear aligners
  • •Residual planned tooth movements no greater than 0.5 mm per tooth per aligner stage
  • •Absence of active periodontal disease at baseline: probing depth 3 mm or less at all sites, and no bleeding on probing at index sampling sites
  • •Written informed consent; for participants aged 15-17 years, written consent from parent or legal guardian is also required

排除标准

  • •Systemic conditions known to affect periodontal tissues (e.g., uncontrolled diabetes mellitus, immunosuppressive therapy)
  • •Antibiotic therapy within the 3 months preceding enrollment
  • •Active gingivitis (modified gingival index 2 or greater) or periodontitis at baseline
  • •Habitual mouth breathing (self-reported or clinically assessed)
  • •Poorly adapted fixed prosthetic restorations adjacent to planned index sampling sites
  • •Visible plaque at more than 50% of tooth surfaces at baseline
  • •Self-reported aligner compliance below 22 hours per day during the study period
  • •Pregnancy or breastfeeding

研究组 & 干预措施

Supragingival Trimming-Line Design

Experimental

Finishing clear aligner with a straight horizontal trimming-line positioned approximately 2 mm apical to the free gingival margin. The aligner edge covers approximately 2 mm of gingival tissue with direct contact, partially enclosing the gingival sulcus entrance, but does not penetrate the sulcus itself. Material: CA Pro tri-layer thermoplastic aligner (SCHEU-DENTAL GmbH, Iserlohn, Germany; CE-marked). Worn 22 hours/day or more during finishing orthodontic treatment. Assigned to the arch with greater planned intrusion; if equal or zero on both arches, assigned by pre-specified systematic alternation in enrollment order.

干预措施: CA Pro tri-layer finishing clear aligner (SCHEU-DENTAL GmbH) (Device)

Juxtagingival Festooned Trimming-Line Design

Active Comparator

Finishing clear aligner with a festooned trimming-line following the natural scalloped contour of the free gingival margin. The aligner edge terminates exactly at the gingival margin without covering gingival tissue and without entering the gingival sulcus, leaving the sulcus entrance accessible to saliva and oxygen. Material: CA Pro tri-layer thermoplastic aligner (SCHEU-DENTAL GmbH, Iserlohn, Germany; CE-marked). Worn 22 hours/day or more during finishing orthodontic treatment. Assigned to the arch with lesser or no planned intrusion; if equal or zero on both arches, assigned by pre-specified systematic alternation.

干预措施: CA Pro tri-layer finishing clear aligner (SCHEU-DENTAL GmbH) (Device)

结局指标

主要结局

Periodontal Pathogen Burden Score per Dental Arch (0-7)

时间窗: 4 weeks and 8 weeks after finishing aligner placement

Number of periodontal pathogen species with quantitative real-time PCR signal exceeding the kit-validated clinical significance threshold per dental arch. Seven species tested: Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, Porphyromonas endodontalis, Fusobacterium nucleatum, Prevotella intermedia. Detected by PeriodontScreen Real-TM assay (Sacace Biotechnologies Srl, Como, Italy; REF T01707-96-S; CE-marked IVD). Score range: 0 (no species above threshold) to 7 (all seven above threshold). Assessed per arch at T1 and T2.

次要结局

未报告次要终点

研究者

发起方
George Emil Palade University of Medicine, Pharmacy, Sciences and Technology of Targu Mures
申办方类型
Other
责任方
Principal Investigator
主要研究者

Emilia Rusu

Doctoral Researcher in Dental Medicine; Senior Specialist in Orthodontics

George Emil Palade University of Medicine, Pharmacy, Sciences and Technology of Targu Mures

研究点 (1)

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