Evaluation of Bacterial Reduction After Pulpectomy in Primary Molars
ConditionIrreversible Pulpitis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age4-6
SponsorCairo University
About this trial
The primary aim of the study is to compare the bacterial reduction in pulpectomy of primary molars using a single rotary file system versus conventional manual instrumentation.
Eligibility criteria
Qualifiers
Children age 4 to 6 years
Medically free children
Cooperative children
Restorable mandibular second primary molars with signs or symptoms of irreversible pulpitis
Disqualifiers
Uncooperative children
Children with systemic disease
Children with physical disability
Children with mental disability
Trial design
Treatments tested in this trial
- Rotary Instrumentation
- Manual Instrumentation
Treatment groups
34 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov