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Comparison of MedCem MTA and Formocresol Used in Pulpotomies in Primary Teeth.

Comparison of MedCem MTA and Formocresol Used in Pulpotomies in Primary Teeth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01962077
Enrollment
60
Registered
2013-10-14
Start date
2013-10-31
Completion date
2021-06-30
Last updated
2021-07-06

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

Conditions

Effectiveness of MedCem MTA® in Pulpotomies Primary Teeth, Pulpotomies Primary Teeth

Keywords

pulpotomy, MTA, primary teeth, formocresol

Brief summary

assess the effect of MedCem MTA as a pulp medicament following pulpotomy in human primary molars with carious pulp exposure in comparison to Formocresol.

Interventions

PROCEDUREMedCem MTA pulpotomies in primary teeth.

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
2 Years to 10 Years
Healthy volunteers
Yes

Inclusion criteria

1. healthy children 2. with Asymptomatic primary molars with a deep carious lesion; 3. Exposure of a vital pulp by caries; 4. No clinical or radiographic evidence of pulp degeneration, such as excessive bleeding from the root canal, internal root resorption, inter-radicular and/or periapical bone destruction,swelling, or sinus tract; 5. Ability to perform a leakage free restoration of the teeth using stainless steel crown, or amalgam/resin based restoration.

Design outcomes

Primary

MeasureTime frameDescription
Success of MedCem MTA pulpotomy in primary molarUp to 36 monthsNo pain, no swelling or sinus tract, no internal root resorption progressing into the bone, no furcation and/or periapical bond destruction.

Countries

Israel

Outcome results

None listed

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