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Clinical Trials in Egypt / NCT07591324
Recruiting Not applicable

the Objective of This Research is to Compare the Clinical Effectiveness of the Conventional Lingual Arch Space Maintainers With Three-dimensional Printed Space Maintainers.

NCT07591324 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-01-22
Last updated
2026-05-15

Condition(s) studied

Gingival HealthSpace MaintenancePain and Anxiety

Investigational drug(s) / intervention(s)

Conventional spacemaintainer3D printed spacemaintainer

Conventional spacemaintainer: Two bands will be selected and checked for fit and adaptation around the distal abutment teeth, then an alginate impression will be taken and will be sent to the laboratory for fabrication

3D printed spacemaintainer: An intraoral scan for the patients' lower arch will be taken using a 3D digital dental scanner.

Study summary

the objective of this research is to compare the clinical effectiveness of the conventional lingual arch space maintainers with three-dimensional printed space maintainers.

Eligibility

Sex
ALL
Min age
7 Years
Max age
9 Years
Healthy volunteers
No
Inclusion Criteria: * Apparently, healthy cooperative children have recently prematurely loss of more than one mandibular primary molar in any of the quadrants, full erupted mandibular first permanent molars in both sides, and whose lower permanent incisors have erupted * 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 * Caries-free and periodontally healthy abutment teeth * Absence of parafunctional habits or abnormal occlusion conditions such as crossbite, open bite, or deep bite. * Children's age ranges from 7 to 9 years-old * Radiographically, presence of permanent successors, more than one millimeter of bone covering the successor tooth germ, and/or only about one-third of the root of the permanent tooth has been formed. * 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 (1)

FacilityCityRegionStatus
Suez Canal University Ismailia Ismailia Governorate Recruiting

More Suez Canal 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 NCT07591324 on ClinicalTrials.gov ↗ ← All trials in Egypt