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3D Printed vs CAD/CAM Rehabilitation of Primary Anterior Teeth Loss

Clinical Evaluation of 3D Printed vs CAD/CAM Rehabilitation of Primary Anterior Teeth Loss

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07752147
Enrollment
40
Registered
2026-08-07
Start date
2025-07-11
Completion date
2026-08-03
Last updated
2026-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Modified Fixed Bridge

Keywords

3D Printed, CAD/CAM, modified fixed bridge, anterior teeth loss

Brief summary

compare 3D Printed versus CAD/CAM fabricated modified fixed appliance for rehabilitation of premature loss of anterior teeth in preschool children

Detailed description

The study will be conducted as a clinical trial and it will be carried out at Pediatric Dentistry Department, Faculty of Dentistry, Tanta University. Forty preschool children from both genders aged from 3-5 years will be included in the study. The selected children will be divided into two groups. Group I: Twenty children will receive 3D Printed modified fixed bridge. Group II: Twenty will receive CAD/CAM fabricated modified fixed bridge. Evaluation of both appliances will be carried out at baseline, 6 and 12 months

Interventions

DEVICE3D Printed modified fixed bridge

the 3D Printed modified fixed appliances compared to CAD/CAM fabricated ones for rehabilitation of premature loss of anterior teeth

DEVICECAD/CAM fabricated modified fixed bridge

the CAD/CAM fabricated modified fixed bridge used a active control

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
3 Years to 5 Years
Healthy volunteers
No

Inclusion criteria

1. Healthy children (ASA I or II) 2. Premature loss of one to four maxillary primary incisors 3. At least 6 months remaining before the expected eruption of the permanent successor 4. Presence of sufficient healthy abutment teeth (primary canines) 5. Adequate oral hygiene (Plaque Index ≤1). 6. Cooperative child (Frankl Behavior Rating 3, 4).

Exclusion criteria

1. Children with craniofacial anomalies or syndromes (e.g., cleft lip and palate). 2. Children with developmental dental anomalies affecting the anterior region (e.g., hypodontia, severe enamel defects). 3. Severe gingivitis or periodontal disease around the abutment teeth. 4. Deep bite, severe malocclusion, or traumatic occlusion that could interfere with appliance function. 5. Parafunctional habits that could increase appliance failure( Bruxism, Nail biting, Biting hard objects). 6. Persistent oral habits that may affect appliance stability

Design outcomes

Primary

MeasureTime frameDescription
Clinical survival rate12 monthsDebonding, breakage of appliance ( failure causes)
Gingival health12 monthsGingival index will be assessed by clinician
Esthetic evaluation12 monthschild and parent evaluation of restoring child esthetics using visual analog scale

Secondary

MeasureTime frameDescription
Questionnaire12 monthsdetermine whether one appliance provides greater improvements in: Eating and chewing ability, Speech, Smile appearance, Child confidence and social interaction, Parent satisfaction and reduced family concern.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026