Digital Versus Conventional Guided Gingivectomy

A

Ain Shams University

Status

Not yet enrolling

Conditions

Altered Passive Eruption of Teeth

Treatments

Procedure: Convectional guided gingivectomy procedure
Procedure: Fully digital guided gingivectomy procedure

Study type

Interventional

Funder types

Other

Identifiers

NCT05969132
FDASU-RecIM122209

Details and patient eligibility

About

The goal of this randomized controlled clinical study is to compare Fully digital to conventional guided Gingivectomy procedure in management of excessive gingival display caused by altered passive eruption type 1A. The main question it aims to answer is: Does the fully digital guided gingivectomy approach able to introduce a more precise, accuracy and reliability technique with more patient satisfaction compared to the conventional guided method?

Full description

Nowadays, the concept of smile and dental esthetics is no longer limited to the teeth. The essentials of a smile involve the relationship between the three primary components: the teeth, lip framework, and the gingival scaffold. The term "pink aesthetics" refers to the aesthetics of gingival tissues, which play a significant influence in smile aesthetics. Excessive gingival display while smiling, also usually known as a "gummy smile," is a common esthetic concern among dental patients and, being largely viewed as unesthetic, leads many patients to seek some form of treatment to address the issue. Gummy smile (Excessive gingival display) is recognized by the American Academy of Periodontology (AAP) as a deformity and mucogingival condition that affects the area around the teeth. This condition could be caused by many etiological factors: short lip, hypermobile/hyperactive lip, short clinical crowns, dentoalveolar extrusion, altered passive eruption (APE), gingival hyperplasia, and vertical maxillary excess. Altered passive eruption defined as "the gingival margin in the adult is located incisal to the cervical convexity of the crown and removed from the cementoenamel junction of the tooth". Altered passive eruption classified into two main classes according to the relationship of the gingiva to the anatomic crown and furthermore subdivided those classes according to the position of the osseous crest. The two types are subdivided into four categories: 1A, 1B and 2A, 2B. The diagnosis of APE is made on a collective clinical and radiographic examination, it begins with analyzing the repose during a natural smile followed by analyzing the gingival display, the alveolar crest level, as well as the lip line of the patient. Determination can be made whether a gingivectomy alone will suffice or a gingival flap will be needed with or without ostectomy will depend of the diagnosis of APE and classification of each case. The selection of one technique over another depends on several patient related factors such as esthetics, clinical crown to root ratio, root proximity, root morphology, furcation location, individual tooth position, collective tooth position and ability to restore the teeth. The gingivectomy approach alone is used when 3 mm gingival tissue or greater exists from bone to gingival crest, and an adequate attached gingiva will remain after surgery (APE type IA). A diagnostic wax-up then an intraoral fabricated mock-up representing the desired outcome can assist in the selection of proper planning of the need for periodontal surgical approach. Diagnostic mock-up fabricated using a temporary bis-acrylic resin with a putty guide directly from the wax-up can be used to provide the patient and clinician with an evaluation of the future outcome and can be used as a surgical guide for gingivectomy procedures. The major limitations with conventional guided gingivectomy procedure would be the time consumed during making and modifying conventional wax-ups as well as the unpredictable estimate of where the gingival margin should be. Utilization of digital workflows allowed the enhancement of communication and might improve the predictability of contemporary gingivectomy approach. The introduction of computer-aided design and computer-aided manufacturing (CAD-CAM) techniques has helped surgeons perform more precise and predictable surgery and contributed to improved esthetics. By combining the use of Digital Smile Design and CAD/CAM technology with (3D) printing, a surgical guide for Gingivectomy procedure could be produced. The aim of the present study will be to evaluate accuracy and reliability of digital guided method of gingivectomy procedure using CAD CAM technology versus conventional method using resin Mock-up as gingivectomy surgical guide. Research Question "Does the fully digital guided gingivectomy approach able to introduce a more precise, accuracy and reliability technique with more patient satisfaction compared to the conventional guided method?"

Enrollment

18 estimated patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients complaining of Excessive gingival display (3mm or more gingival display at full smiling)
  • Patients classified as Altered Passive Eruption Type 1A

Exclusion criteria

  • Patients need restorative or orthodontic correction.
  • Pregnant and lactating females.
  • Heavy smoker ≥ 10 cigarettes/day.
  • Poor oral hygiene.
  • Patients with systemic diseases which could influence the outcome of the therapy e.g.

(Diabetic patients).

  • Heavy smoker ≥ 10 cigarettes/day.
  • Vulnerable groups of patients e.g. (prisoners, handicapped patients and decisionally impaired individuals)

Trial design

18 participants in 2 patient groups

Digital workflow-based Protocol
Experimental group
Description:
Fully digital guided gingivectomy procedure
Treatment:
Procedure: Fully digital guided gingivectomy procedure
Mock-up workflow-based Protocol
Active Comparator group
Description:
Convectional guided gingivectomy procedure
Treatment:
Procedure: Convectional guided gingivectomy procedure

Trial contacts and locations

0

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Central trial contact

Doaa A. Khattab, Ass. Prof.; Eslam O. Hashem, Master st.

Data sourced from clinicaltrials.gov

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