NCT05945758

Brief Summary

injectable resin composite technique will show a better clinical and esthetic performance compared to conventional layering resin composite technique in patients with multiple spacing in the maxillary anterior teeth area or not.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2023

Typical duration for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 4, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

July 14, 2023

Completed
18 days until next milestone

Study Start

First participant enrolled

August 1, 2023

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

July 14, 2023

Status Verified

July 1, 2023

Enrollment Period

2.2 years

First QC Date

July 4, 2023

Last Update Submit

July 12, 2023

Conditions

Keywords

injectable resin compositeconventional layering techniqueFDImultiple spacing

Outcome Measures

Primary Outcomes (1)

  • Change from baseline in Esthetic anatomical form at 6,12,18& 24 months.

    FDI criteria. Possible scores range from 1 (Excellent) to 5 (Immediate replacement necessary).

    T1: Baseline. T2: 6 months. T3: 12 months. T4: 18 months. T5: 24 months.

Secondary Outcomes (3)

  • Change from baseline in Color match and translucency at 6,12,18& 24 months.

    T1: Baseline. T2: 6 months. T3: 12 months. T4: 18 months. T5: 24 months.

  • Change from baseline in Surface and marginal staining at 6,12,18& 24 months.

    T1: Baseline. T2: 6 months. T3: 12 months. T4: 18 months. T5: 24 months.

  • Change from baseline in Surface lustrous at 6,12,18& 24 months.

    T1: Baseline. T2: 6 months. T3: 12 months. T4: 18 months. T5: 24 months.

Study Arms (2)

Spacing in the maxillary anterior teeth area treated with injectable resin composite technique.

EXPERIMENTAL

The injectable composite resin technique is an indirect/direct method that uses a transparent silicone index for accurate and predictable translation of diagnostic wax-up into composite restorations without the need for tooth preparation. The Spaces will be restored with injectable resin composite.

Procedure: Injectable resin composite technique.

Spacing in the maxillary anterior teeth area treated with conventional layering composite technique.

ACTIVE COMPARATOR

shade mapping of enamel and dentin, then isolation the teeth with rubber dam. Palatal index will be done on waxing up and applied against the palatal surface to check the adaptation of the index. Then, the enamel shade adapted on the index in the spacing area. index will be placed back on the anterior teeth to build the palatal wall. A brush will be used to adapt the composite to the margin. After removing excess material, light curing will be carried out for 20 seconds. The Unica matrix (Polydentia) will be used to restore the proximal wall, and to achieve a good seal with the palatal wall. The matrix can be stabilized with a wedge if necessary. Building the proximal wall using the enamel shade, and the incisal halo by using a dentin shade, the frame to layer the core of the restoration will be ready.

Procedure: Conventional layering technique

Interventions

A metal impression tray was filled with transparent vinyl polysiloxane (EXACLEAR, GC) and used to copy the stone model with the wax-up. Then, the replica will be separated from metal tray and a needle-shaped bur will be used to drill holes through the silicone key ending in the middle of the incisal edge. It will be checked whether the holes were large enough to enable the tip of the composite syringe to pass easily and completely. Neighbouring teeth (mesial and distal one) isolated using Teflon tape, as each tooth will individually be restored for establishment of satisfactory contact points. Following etching and rinsing, the tooth dried, and a dental cord (Ultrampak, Ultradent) will be packed into sulcus for mechanical prevention of subgingival composite flow. Then, the transparent silicone index will be placed in the correct intraoral position, and a syringe filled with flowable composite will be inserted through the hole on the incisal edge.

Also known as: Beautiful Flow Plus F03, Medium Viscosity, Shofu Dental
Spacing in the maxillary anterior teeth area treated with injectable resin composite technique.

the palatal surface will be restored by enamel shade; adapted on the index in the spacing area then The Unica matrix (Polydentia) will be used to restore the proximal wall, and to achieve a good seal with the palatal wall. The matrix can be stabilized with a wedge if necessary. Building the proximal wall using the enamel shade, and the incisal halo by using a dentin shade, the frame to layer the core of the restoration will be ready.

Also known as: Enamel and Dentin shades
Spacing in the maxillary anterior teeth area treated with conventional layering composite technique.

Eligibility Criteria

Age20 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Sound and vital upper anterior teeth.
  • Spacing in the maxillary anterior teeth area ranging from .5mm to 2mm.
  • Minor misalignment, correction of peg laterals.

You may not qualify if:

  • Non-vital, fractured, or cracked teeth.
  • Teeth with caries or in need of replacement of existing restorations.
  • Rampant caries, atypical extrinsic staining of teeth.
  • Heavy occlusion and occlusal contacts or history of bruxism.
  • Severe periodontal affection.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle investigator

Study Record Dates

First Submitted

July 4, 2023

First Posted

July 14, 2023

Study Start

August 1, 2023

Primary Completion

October 1, 2025

Study Completion

December 1, 2025

Last Updated

July 14, 2023

Record last verified: 2023-07