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Clinical Outcomes of Bio-MA and ProRoot MTA in Endodontic Treatment

M

Mahidol University

Status

Enrolling

Conditions

Clinical Outcome
Endodontic Disease

Treatments

Other: Calcium silicate cement

Study type

Interventional

Funder types

Other

Identifiers

NCT04243993
MU-DT/PY-IRB 2016/052.0310

Details and patient eligibility

About

The purpose of this study is to compare the endodontic outcomes of Bio-MA and ProRoot MTA in pulpotomy, orthograde MTA apical barrier, root perforation repair, endodontic microsurgery.

Full description

The patients were recruited at the Endodontic clinic, Faculty of Dentistry, Mahidol University, Thailand. Each treatment was provided following the standard protocol. The calcium silicate based material (Bio-MA or ProRoot MTA) was randomly selected and used in the treatment. The patients were periodically recalled at 6 to 12 months. The outcome of the three treatments based on the clinical and radiographic criteria was assessed by the calibrated examiners and interpreted as ''healed/healing" or ''disease.''

Enrollment

60 estimated patients

Sex

All

Ages

10 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Teeth treated with pulpotomy, orthograde MTA apical barrier, root perforation repair or endodontic microsurgery

Exclusion criteria

  • Teeth with un-restorable condition
  • Teeth with crack or fracture
  • Teeth with external or internal root resorption
  • Teeth with chronic periodontitis with marginal bone loss more than 5 mm

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Bio-MA
Other group
Description:
Calcium silicate cement containing calcium chloride accelerator
Treatment:
Other: Calcium silicate cement
ProRoot MTA
Other group
Description:
Calcium silicate cement without calcium chloride accelerator
Treatment:
Other: Calcium silicate cement

Trial contacts and locations

1

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Central trial contact

Danuchit Banomyong, Ph.D.

Data sourced from clinicaltrials.gov

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