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Comparison of pain in root canal therapy of primary teeth in one or two visit

Not Applicable
Conditions
Pulp therapy in primary.
Pulpitis
Registration Number
IRCT2016122231473N1
Lead Sponsor
Research and Technology Vice Chancellry, Kerman University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

vital decidious teeth with active bleeding during access cavity preparation,  lack of clinical and radiographic evidence of pulpal necrosis,  resorption of less than two third of the root length, restoration possible, cooperative child, at least one molar with evidence of irreversible pulpitis , e.g. sensitivity to cold or hot stimulus.
Exclusion criteria: child with systemic diseases, follicular or dentigerous cyst below decidous tooth, pathologic resorption of at least one third of root length with fistulous sinus tract, resorption of more than two third of root length, isolation of tooth not possible, advanced internal resorption, periradicular lucency involving permanent tooth bud.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain relief after visit. Timepoint: one day-seven days. Method of measurement: VAS.
Secondary Outcome Measures
NameTimeMethod
Pain relief. Timepoint: 1-7 day. Method of measurement: VAS.
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