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A comparison of success rate of two dental bioceramic cements used in vital pulp therapy

A randomized controlled trial on the clinical success rate of vital pulp therapy using calcium silicate based bioceramic and ProRoot MTA on permanent and primary teeth.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0005734
Enrollment
200
Registered
2021-01-04
Start date
2020-12-28
Completion date
Unknown
Last updated
2021-01-06

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

Conditions

None listed

Interventions

Medical Device : 1) Endocem MTA Premixed - Inserted in cavity 2) ProRoot MTA - Inserted in cavity In both case, same procedure of partial pulpotomy has done

Sponsors

Yonsei University Health System, Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Pulp exposured matured tooth or primary tooth with ? Normal mobility and percussion ? without unknown pain ? Hemostasis can be done within 3-5 minutes with wet cotton ? No internal root resorption observed ? No periapical radiolucency ? Available to restore with composite resin or indirect restoration(Permanent tooth), Crown restoration(Primary tooth)

Exclusion criteria

Exclusion criteria: ? Spontaneous pain ? Unusual mobility and percussion test result ? Swelling or sinus tract on gum ? No tooth vitality observed ? Fail to hemostasis 5 minutes after pulpotomy

Design outcomes

Primary

MeasureTime frame
Pulp survival rate

Secondary

MeasureTime frame
Tooth survival rate

Countries

Korea, Republic of

Contacts

Public ContactJunghoon Lee

Yonsei University Health System, Dental Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026