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Evaluation of success & failure of Mineral Trioxide Aggregate (MTA) & Biodentine in pulp therapy of second mandibular primary molar with irreversible pulpitis

Phase 2
Recruiting
Conditions
Irreversible pulpitis of second mandibular primary molar.
Pulpitis
K04.0
Registration Number
IRCT20210419051016N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

No underlying systematic diseases which leads to inhibition of local anesthesia injection
Having a vital second mandibular primary molar tooth with deep caries lesion in the crown that is not extended subgingivally more than 1 mm
Having the history of typical pain related to the irreversible pulpitis (patient's chief complaint is spontaneous pain that lasts more than multiple seconds)
Sensitivity to thermal stimuli
All teeth are vital and the operator evaluates the pulp vitality by visual observation of pulp hemorrhage from all root canals of the intended tooth
Having access to the participant for 12-months follow-up
Pulp exposure due to severe carious crown
No pathologic mobility
No abscess, fistula, or swelling related to the intended tooth
Possibility of restoration with Stainless Steel Crown (SSC)
Possibility of providing hemostasis in the orifice entrance
No internal or pathologic external root resorption
No periapical radiolucency
No widening in the periodontal ligament
No radiolucency in furcation area
No calcific degeneration of the pulp
No root resorption more than 1/3 of the root length

Exclusion Criteria

Patients with underlying systemic disorders, physical, or mental disabilities
Presence of any clinical or radiographic sign of pulpal degeneration including severe hemorrhage from root canals that making hemostasis impossible in 5 minutes, internal root resorption, bone resorption in furcation or preapical area, swelling or sinus tract formation, and pulp necrosis
Physiologic root resorption more than 2/3 of the root length (the sign of exfoliation)
Non-physiologic root resorption
Non-restorable tooth

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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