此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Comparison of Dual Digitally Guided vs Conventional Crown Lengthening (DIGICROWN)

2026年9月2日 更新者:Arab International University

Randomized Controlled Trial Evaluating Digital Dual Surgical Guide in Esthetic Crown Lengthening

This randomized controlled clinical trial aims to evaluate the clinical performance and patient-centered outcomes of dual digitally guided crown lengthening compared to the conventional surgical technique in the management of gummy smile caused by altered passive eruption (Type B1).

A total of 18 patients will be randomly allocated into two groups: the control group will undergo conventional crown lengthening based on clinical measurements, while the intervention group will receive crown lengthening using a dual digitally fabricated surgical guide.

The primary outcome is the gain in clinical crown length at 3 months. Secondary outcomes include operating time, pain perception, patient satisfaction, gingival margin stability, and periodontal clinical parameters.

This study aims to determine whether digital guidance improves surgical accuracy, efficiency, and patient satisfaction compared to traditional techniques

研究概览

详细说明

Esthetic crown lengthening is a commonly performed periodontal surgical procedure indicated for the correction of excessive gingival display, particularly in cases of altered passive eruption. Achieving optimal esthetic outcomes requires precise determination of gingival and osseous resection levels, which can be challenging using conventional clinical methods.

With the advancement of digital dentistry, computer-aided design and manufacturing (CAD/CAM) technologies have enabled the development of digitally guided surgical approaches. The dual digitally guided technique integrates two levels of guidance to control both soft tissue and bone resection, potentially enhancing surgical precision and predictability.

This randomized controlled clinical trial is designed to compare the effectiveness of dual digitally guided crown lengthening with the conventional technique in patients presenting with gummy smile due to altered passive eruption (Type B1).

Eighteen systemically healthy patients aged 18-40 years will be recruited and randomly assigned into two equal groups. The control group will undergo conventional crown lengthening using clinical measurements and manual surgical techniques. The intervention group will be treated using a dual digitally fabricated surgical guide based on digital smile design, CBCT analysis, and intraoral scanning.

Clinical and patient-reported outcomes will be assessed at baseline and during follow-up periods. The primary outcome is the gain in clinical crown length measured at 3 months postoperatively. Secondary outcomes include operating time, pain (VAS), patient satisfaction (VAS), gingival margin level, probing depth, gingival index, plaque index, bleeding on probing, keratinized gingival height, and gingival thickness.

The results of this study are expected to provide evidence regarding the benefits of digital guidance in periodontal esthetic surgery and its potential to improve clinical outcomes and patient experience.

研究类型

介入性

注册 (实际的)

18

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Damascus、叙利亚
        • School of Dental Medicine

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Patients presenting with gummy smile due to altered passive eruption (Type B1)
  • Presence of at least 6 maxillary anterior teeth indicated for crown lengthening
  • Good oral hygiene and ability to maintain plaque control
  • Systemically healthy patients

Exclusion Criteria:

  • Poor oral hygiene
  • Smokers
  • Pregnancy or lactation
  • Systemic diseases affecting periodontal tissues
  • Previous periodontal surgery in the study area
  • Active periodontal disease
  • Presence of periapical pathology in the study area
  • Ongoing orthodontic treatment
  • Gummy smile due to skeletal or muscular causes

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
有源比较器:Conventional Crown Lengthening
Participants in this group will undergo conventional surgical crown lengthening based on clinical evaluation and manual measurements. The procedure includes gingivectomy and osseous resection performed according to standard periodontal surgical protocols without the use of digital guidance.
Conventional surgical crown lengthening performed based on clinical examination and manual measurements. The procedure includes gingival recontouring and osseous resection carried out according to standard periodontal surgical protocols without the use of digital guidance.
实验性的:Dual Digitally Guided Crown Lengthening
Participants in this group will receive crown lengthening using a dual digitally fabricated surgical guide. The procedure is planned using digital smile design, intraoral scanning, and CBCT analysis to guide both soft tissue and bone resection, aiming to improve surgical precision and predictability.
Crown lengthening performed using a dual digitally fabricated surgical guide. The procedure is planned using digital smile design, intraoral scanning, and CBCT imaging to guide both soft tissue and bone resection, enhancing surgical accuracy and predictability.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Gain in Clinical Crown Length
大体时间:Baseline and 3 months postoperatively
Change in clinical crown length (mm), measured from the incisal edge to the gingival margin using a periodontal probe, to assess the effectiveness of crown lengthening procedures.
Baseline and 3 months postoperatively

次要结果测量

结果测量
措施说明
大体时间
Surgical Operating Time
大体时间:During surgery (intraoperative)
Total duration of the surgical procedure measured in minutes from the first incision to completion of osteotomy.
During surgery (intraoperative)
Relative Gingival Margin Level
大体时间:Baseline, 1 week, and 3 months postoperatively
Measurement of gingival margin position (mm) relative to a fixed reference point to evaluate soft tissue stability.
Baseline, 1 week, and 3 months postoperatively
Probing Depth
大体时间:Baseline and 3 months postoperatively
Periodontal probing depth (mm) measured at standardized sites using a periodontal probe.
Baseline and 3 months postoperatively
Gingival Index (GI)
大体时间:Baseline and 3 months postoperatively
Assessment of gingival inflammation using the Gingival Index scoring system.
Baseline and 3 months postoperatively
Plaque Index (PI)
大体时间:Baseline and 3 months postoperatively
Assessment of oral hygiene status using the Plaque Index scoring system.
Baseline and 3 months postoperatively
Bleeding on Probing (BOP)
大体时间:Baseline and 3 months postoperatively
Presence or absence of bleeding upon gentle probing, expressed as a percentage of bleeding sites.
Baseline and 3 months postoperatively
Keratinized Gingival Height
大体时间:Baseline, 1 week, and 3 months postoperatively
Width of keratinized gingiva (mm) measured from the gingival margin to the mucogingival junction.
Baseline, 1 week, and 3 months postoperatively
Gingival Thickness
大体时间:Baseline and 3 months postoperatively
Thickness of gingival tissue (mm) measured using transgingival probing or ultrasound methods.
Baseline and 3 months postoperatively
Postoperative Pain (Visual Analog Scale)
大体时间:24 hours, 7 days, and 14 days postoperatively
Patient-reported pain assessed using a Visual Analogue Scale (VAS) ranging from 0 (no pain) to 10 (worst pain imaginable).
24 hours, 7 days, and 14 days postoperatively
Patient Satisfaction (Visual Analog Scale)
大体时间:7 days and 3 months postoperatively
Patient satisfaction with the esthetic and functional outcome measured using a Visual Analogue Scale (VAS).
7 days and 3 months postoperatively

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Raghad Alrefaai, DDs、Damascus University
  • 学习椅:Razan Khattab, PhD、Damascus University
  • 研究主任:Saleh Al Kurdi, PhD、Arab International University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2024年7月1日

初级完成 (实际的)

2025年10月15日

研究完成 (实际的)

2026年2月25日

研究注册日期

首次提交

2026年5月4日

首先提交符合 QC 标准的

2026年5月4日

首次发布 (实际的)

2026年5月8日

研究记录更新

最后更新发布 (实际的)

2026年9月4日

上次提交的符合 QC 标准的更新

2026年9月2日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • DN-10062024-3764

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅