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Partial pulpotomy on caries free human teeth using iRootBP and White ProRoot MTA: a randomized controlled trial

Phase 2
Conditions
pulp inflammation.
Necrosis of pulp
Registration Number
IRCT201102145804N2
Lead Sponsor
Vice chancellor for research of Islamic Azad University, Dental Branch, Tehran
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
24
Inclusion Criteria

Patients who are assigned to extract two premolar teeth in one jaw for orthodontic treatment plan will be included; Their parents need to read and sign a fully informed form; They shouldn't have any systematic complication or take any medicine during the period of study; The teeth need to be free of any symptom, caries and decalcification; They should give a normal response to pulp sensitivity tests (cold test) compared to the control tooth on the same quadrant; The teeth need to be free of mobility or swelling in the surrounding soft tissues and any sensitivity on palpation or percussion; On radiographic examination no apical lucency or PDL widening should be detected.
Exclusion criteria: Any sign of crack; filling; caries or hypocalcification on teeth will cause exclusion. Also the teeth showing apical lucency or PDL widening will be excluded; Any sensitivity to cold, heat or bite will lead to exclusion; The responses beyond the normal limits to pulp vitality testing and any medicine consumption would cause exclusion.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dentinal bridge formation. Timepoint: six weeks after intervention. Method of measurement: microscopic evaluation.;Appearance of the dentinal bridge compared to normal dentin. Timepoint: six weeks after intervention. Method of measurement: microscopic evaluation of appereance of the dentinal bridge compared to normal dentin.;Thickness of the dentinal bridge compared to normal dentin. Timepoint: six weeks after intervention. Method of measurement: microscopic evaluation of thickness of the dentinal bridge compared to normal dentin.
Secondary Outcome Measures
NameTimeMethod
Inflammatory status of the pulp. Timepoint: six weeks after intervention. Method of measurement: microscopic evaluation : inflammatory cell count and their distribution.
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