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Space Changes After Premature Loss of Lower First Primary Molars in Children Using Digital Scanning

The Space Changes Following Premature Loss of Lower First Primary Molars in the Primary Dentition Stage Using Digital Scanning A Prospective Split-mouth Clinical Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06965777
Enrollment
11
Registered
2025-05-11
Start date
2025-08-01
Completion date
2026-03-01
Last updated
2025-05-14

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

Conditions

Dental Arch Development, Pediatric Tooth Extraction, Premature Loss of Primary Molars, Space Maintenance

Keywords

Tooth Loss, Dental Arch, Pediatric Dentistry, Primary Dentition

Brief summary

This prospective split-mouth clinical study aims to evaluate space changes in the mandibular dental arch following premature extraction of the lower first primary molar in children aged 3 to 5.5 years. Using digital 3D models, changes in the D space and mandibular arch perimeter will be measured at baseline and 6 months post-extraction. The goal is to determine whether space maintainers are necessary in the primary dentition stage.

Detailed description

Premature loss of primary molars in children is a common result of caries or trauma, potentially affecting future occlusion and alignment. This study investigates the space changes that occur after unilateral premature extraction of the mandibular first primary molar before the eruption of the permanent first molar. Using a split-mouth design, the contralateral non-extracted side serves as the control. Digital impressions will be taken at baseline (day of extraction) and after 6 months. The primary outcome is the change in the D space, and the secondary outcome is the change in the mandibular arch perimeter, both measured using 3D digital software. The study aims to provide evidence for or against the routine use of space maintainers in similar clinical scenarios, potentially reducing unnecessary treatment and improving patient comfort.

Interventions

None listed

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Years to 66 Months
Healthy volunteers
Yes

Inclusion criteria

* Children aged 3 to 5.5 years * Mandibular first primary molar indicated for extraction due to extensive decay or hopeless prognosis * Contralateral mandibular first primary molar must be intact and free of proximal caries * No eruption of mandibular permanent first molar at the time of enrollment * Presence of primary canines and second primary molars * No space maintainers placed * Parents/caregivers unable or unwilling to fabricate a space maintainer

Exclusion criteria

* Bilateral premature loss of mandibular first primary molars * Contralateral mandibular molar has proximal caries or poor prognosis * Children with good prognosis first primary molars (i.e., not needing extraction) * Eruption of the mandibular permanent first molar * Children who already have space maintainers * Uncooperative behavior preventing study participation

Design outcomes

Primary

MeasureTime frameDescription
Change in D Space (Mandibular Arch)Baseline (Day of Extraction) and 6 Months Post-ExtractionThe change in D space (distance between the mesial midpoint of the second primary molar and the distal midpoint of the primary canine) on the extraction side of the mandibular arch. Measured in millimeters using 3D digital models.

Secondary

MeasureTime frameDescription
Change in Mandibular Arch PerimeterBaseline (Day of Extraction) and 6 Months Post-ExtractionThe change in the total arch perimeter of the mandibular arch measured using 3D digital models. The arch perimeter is calculated as the sum of linear segments across reference tooth landmarks. Measured in millimeters.

Countries

Egypt

Contacts

Primary ContactDania Yaser Rahhal Y Rahhal, BDS
dania.rahhal96@hotmail.com+201029020795

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026