Comparative Evaluation of Pulpotomized Primary Molars With Mineral Trioxide Aggregate and New Endodonthic Cement

Comparative Evaluation of Pulpotomized Primary Molars With Mineralized Trioxide Aggregate & New Endodonthic Cement

Status

UNKNOWN

Phases

Phase 3

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00802256

Enrollment

Registered

2008-12-04

Start date

2008-10-31

Completion date

2009-12-31

Last updated

2009-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulpotomy Treatment

Keywords

pulpotomy, primary molar teeth, MTA, NEC, CEM, Primary Molar Teeth Which Require Pulpotomy Treatment

Brief summary

A new Endodontic Cement (NEC) is being compared with mineral trioxide aggregate in pulpotomy of primary molars.

Detailed description

Forty patient are selected randomly. Each patient has at least 2 teeth which require pulpotomy treatment. After removing of carious teeth by a low speed round bur and pulp exposure, roof of pulp chamber is removed completely by a high speed 008 fissure bur. Life tissues of pulp are removed by sharp excavator and rinsing with normal salin. Hemostat is achieved and cavity will be cleaned by 0.5% hypo chlorate solution. MTA or NEC material is mixed according to manufacturer instruction and will be placed in pulp chamber and over pulpal canal orifices for at least 1 mm. The light cure glass inomor is also mixed according to manufacturer instruction and is places over the A or B material and cured for 40 minutes. The treated tooth will be restored with a stainless steel crown or amalgam filling material.

Interventions

PROCEDUREpulpotomy

removal of caries and cronal pulp tissue and then restoring of tooth

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

4 Years to 8 Years

Healthy volunteers

Yes

Inclusion criteria

* Vital pulp exposure of teeth with caries or trauma * No clinical signs & symptoms like pain,inflammation * No radiographic signs & symptoms like: internal resorption,external resorption, furcation involvement,pulp canal obliteration. * The restorable tooth * No dental treatment contraindication

Exclusion criteria

* Systemic diseases * Existence of pain,inflammation or sinus tract * No patient compliance

Design outcomes

Primary

Measure	Time frame
Clinical features and radiographic examination	6 monthes and one year

Countries

Iran

Contacts

Primary ContactFatemeh Shekarchi, student

fshekarchi84@yahoo.com00989124849179

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026