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Clinical Trials in Egypt / NCT06825273
Recruiting Not applicable

Clinical Evaluation of 3-D Printed Partial Denture Space Maintainer

NCT06825273 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-03-01
Last updated
2025-04-17

Condition(s) studied

Space MaintenanceGingival Health

Investigational drug(s) / intervention(s)

space maintainerspace maintainer

space maintainer: 3-D printed partial denture space maintainer will designed for each child patient who has premature loss of primary teeth after doing intraoral scanning

space maintainer: a conventional impression will be done for a child patient with premature loss of his primary teeth, then a plaster model will gained. A conventional acrylic partial denture will be designed and delivered to the patient.

Study summary

Primary dentition is the most suitable space maintainer for permanent teeth. However, as infants often lose their primary teeth too soon, using a space maintainer is the most efficient, long-lasting, and economical way to prevent malocclusions and function impairment in the future. Regarding personalized appliances, space maintainers in digital pediatric dentistry have made significant progress. Digital technology decreases the manual manufacturing stages that take a long time and increases the reliability and durability of digital fabrication procedures.

Eligibility

Sex
ALL
Min age
7 Years
Max age
9 Years
Healthy volunteers
No
Inclusion Criteria: * apparently, healthy cooperative children having recent premature loss of lower primary molars * the permanent successors of the lost primary molars were not expected to erupt within 6 months * Angle's class 1 occlusion with normal primary molar relation * Presence of teeth on the mesial and distal side of the edentulous area * Absence of para-functional habits or abnormal occlusion conditions such as crossbite, open bite, or deep bite. * Radiographically, presence of permanent successors. * parents and children were accepting the new treatment modality. Exclusion Criteria: * children exhibited poor oral hygiene, para-functional oral habits, severe crowding, space loss, and abnormal occlusion * Extraction of primary molars exceeding three months. * Radiographically, absence of permanent successor. * uncooperative children

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
pediatric dentistry department, faculty of dentistry, Tanta university Tanta Egypt Recruiting
Tanta University Tanta Egypt Not Yet Recruiting

More Tanta University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06825273 on ClinicalTrials.gov ↗ ← All trials in Egypt