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This is a study comparing the efficiency of two different oral appliance that is used to preserve the space for the erupting permanent teeth

Phase 3
Registration Number
CTRI/2024/02/062845
Lead Sponsor
Ayesha Fathima S
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Clinical criteria:

Systemically healthy children.

Grossly mutilated or resorbed primary molars bilaterally requiring extraction before the complete eruption of permanent mandibular anteriors.

Sound and healthy teeth adjacent to the extraction site.

No abnormal dental conditions such as crossbite, open bite,

and deep bite.

Radiographic criteria:

Presence of succedaneous tooth bud.

Presence of at least 1 mm bone overlying the succedaneous

Tooth germ with less than one-third of the root formed.

Exclusion Criteria

Parents who didn’t give consent

Individuals having systemic diseases or severe medically compromised.

Grossly carious teeth were adjacent to the created space.

Absence of teeth on the mesial or distal side of the teeth to be extracted

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Survival rateTimepoint: Baseline, 1 month, 3 months, 6 months and 9 months
Secondary Outcome Measures
NameTimeMethod
Gingival health, Incidence of caries in abutment tooth, Space lossTimepoint: Baseline, 1 month, 3 months, 6 months and 9 months
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