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Comparison success rate of TheraCal-LC® ? Mineral Trioxide Aggregate in pulpotomy of primary teeth

Comparison clinical and radiographic success rate of TheraCal-LC® and Mineral Trioxide Aggregate in pulpotomy of primary teeth with 12 month follow up: A split-mouth randomized controlled clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100125003168N7
Enrollment
45
Registered
2020-03-03
Start date
2020-04-05
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

Reversible Pulpitis. Pulpitis

Interventions

Intervention group:.

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 8 Years

Inclusion criteria

Inclusion criteria: -Complete physical and mental health, with no confounding history of allergic reactions and systemic disease and/or use of special local or systemic drugs Having a pair of symmetric primary molar teeth (first or second) in one jaw, having deep caries and vital pulp which is capable of being restored by SSC No history of spontaneous pain, pathologic mobility, draining sinus tract, redness or swelling of vestibule Normal gingival and periodontal condition, with no sensitivity to vestibular palpation, and no pain on percussion test 5-8 years old children No sign of radiolucency in periapical or furcation area No widening of PDL space or loss of lamina dura continuity No evidence of internal/external pathologic root resorption

Exclusion criteria

Exclusion criteria: Lack of informed consent by the child patient’s parent- Abnormal bleeding at the site of pulp exposure (i.e. bleeding with dark color which lasts for more than 5 minutes despite application of wet cotton pellet with mild pressure)

Design outcomes

Primary

MeasureTime frame
Dental pulp vitality after treatment. Timepoint: 6 &12 months. Method of measurement: Lack of any of clinical or radiographic signs or symptoms of treatment failure.

Secondary

MeasureTime frame
Radiographic success. Timepoint: 6&12 months. Method of measurement: Presence of one or more of the following radiographic signs will be considered as failure of treatment: internal and/or external root resorption, periodontal space widening, inter-radicular radiolucency, and periapical lesions.;Clinical success. Timepoint: 6 &12 months. Method of measurement: Presence of one or more of the following clinical signs/symptoms will be considered as failure of treatment: spontaneous pain, swelling, pathologic mobility, tenderness to pressure, and presence of sinus tract, swelling, and sensitivity to percussion.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Leila Erfanparast

Tabriz University of Medical Sciences

leilaerfan@gmail.com+98 413355965

Outcome results

None listed

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