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Clinical Trials/NCT06047925
NCT06047925
Active, not recruiting
Not Applicable

3D-printed Crowns Versus Prefabricated Stainless-Steel Crowns for Intermediate Restoration of Compromised First Permanent Molars (Randomized Controlled Clinical Trial)

Ain Shams University1 site in 1 country40 target enrollmentStarted: June 1, 2023Last updated:

Overview

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
40
Locations
1
Primary Endpoint
The clinical performance of 3d printed crowns versus prefabricated SSCs in compromised first permanent molars

Overview

Brief Summary

The study will evaluate the clinical performance and both patient and parent satisfaction of 3d printed crowns versus prefabricated Stainless-steel crowns (SSCs) in compromised first permanent molars

Detailed Description

A total of Forty permanent first mandibular molars in healthy subjects will be selected from the Pediatric Dentistry and Dental Public Health outpatient clinic.

The molars will be randomly assigned equally into two treatment groups group A 3D-printed crowns & group B prefabricated SSCs, removal of caries with a high-speed handpiece then removal of the remaining carious lesion with excavator then glass ionomer restoration will be placed, preparation of SSCs crowns will be done in Group A by reduction of occlusal surface by about 1.5 mm, Proximally, tooth reduction is made through the mesial and distal contact areas, then roundation of line angles. Proper size of crown will be selected. It can also be helpful to measure the dimension of the contralateral tooth. A correctly fitting crown should snap or click at try in. In group B reduction will be performed on the occlusal surface using a flame stone or a wheel stone, to perform occlusal clearance. Reduction will be performed on the mesial, distal, buccal, and lingual surfaces of the tooth Then roundation of the line angles will be performed. Impression for the preparation will be taken using putty and light poly vinyl siloxane material. The preparation will be optically scanned in the lab and the restoration will be digitally designed using computer designing software. The crown will be printed using 3D printer using hybrid resin material. Crown will be checked for proper fit and cemented to the tooth by self-etch adhesive.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

Double (Investigator-outcome Assessor)

Eligibility Criteria

Ages
10 Years to 13 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Children included in the study should conform to the following criteria:
  • Badly broken-down endodontically treated first permanent molar
  • First permanent molar with extensive multi-surface caries.
  • First permanent molar with structural developmental defects such as hypoplasia, Molar-Incisor Hypomineralization (MIH), Amelogenesis Imperfecta, and Dentinogenesis Imperfecta

Exclusion Criteria

  • Children who are uncooperative needing sedation or general anesthesia.
  • Children who are physically or mentally disabled or having any medical condition that will complicate the treatment.
  • Molars of poor prognosis

Outcomes

Primary Outcomes

The clinical performance of 3d printed crowns versus prefabricated SSCs in compromised first permanent molars

Time Frame: 3,6,12 and 18 months

Evaluation of clinical performance of both crowns regarding gingival health (gingival \& plaque index) and Fracture, retention, marginal discoloration and surface texture according to the modified United states Public Health Service (USPHS) criteria. 3,6-12 and 18 months.

Secondary Outcomes

  • Patient and parent satisfaction.(Immediately ,3,6,12&18 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dina Bassam Mohamed Ahmed

Asisstant lecturer

Ain Shams University

Study Sites (1)

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