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Evaluation of clinical and radiographic success and failure of Mineral Trioxide Aggregate (MTA) and Cold ceramic in pulp therapy of mandibular primary molars with reversible pulpitis in 3-6 years old children: a randomized clinical trial

Evaluation of clinical and radiographic success and failure of Mineral Trioxide Aggregate (MTA) and Cold ceramic in pulp therapy of mandibular primary molars with reversible pulpitis in 3-6 years old children: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230719058851N1
Enrollment
50
Registered
2023-07-27
Start date
2023-08-06
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Mandibular molars reversible pulpitis. Pulpitis

Interventions

Intervention 1: Intervention group A:First, a periapical radiograph will be prepared from the desired tooth using the standard parallel technique with the help of Rinne xcp (dentsply, USA). Film numbe

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: The presence of two-thirds of the root length in terms of radiography; and lack of radiographic evidence of pulp degeneration, such as internal or external root resorption, furca radiolucency, intraradicular or periapical bone destruction, pulp stones. Includes patients who have no systemic diseases such as congenital or rheumatic heart disease, leukemia, allergic reactions to substances such as local anesthetics and latex. They have good individual and family cooperation, deep pitted lesions whose pulp is exposed during caries removal.

Exclusion criteria

Exclusion criteria: The presence of any clinical and radiographic symptoms indicating pulpal degeneration or physiological analysis of more than 2/3 of the root (imminence of tooth loss) non-physiological analysis of the root or possibility of proper tooth restoration.

Design outcomes

Primary

MeasureTime frame
Frequency of pain in treated molars. Timepoint: 3,6 and 12 months after treatment. Method of measurement: The history of the presence or absence of spontaneous pain after the treatment is asked from the patient. (Yes/No).;The frequency of occurrence of sensitivity to dex in treated primary molars. Timepoint: 3,6 and 12 months after treatment. Method of measurement: During a clinical examination with a precision test, the patient is asked if there is any sensitivity or not.;The frequency of occurrence swelling in treated primary molars. Timepoint: 3,6 and 12 months after treatment. Method of measurement: A clinical examination is performed to detect the presence or absence of swelling.;The frequency of occurrence fistula in treated primary molars. Timepoint: 3,6 and 12 months after treatment. Method of measurement: A clinical examination is performed to detect the presence or absence of fistula.;The frequency of occurrence pathologic mobility in treated primary molars. Timepoint: 3,6 and 12 months after treatment. Method of measurement: A clinical examination is performed to detect the presence or absence of pathologic mobility.;The frequency of occurrence of root lucency in radiographic images in treated primary molars. Timepoint: 6 and 12 month after treatment. Method of measurement: Radiographic examination is performed to detect the presence or absence of lucency around the root.;The frequency of occurrence of internal resorbtion in radiographic images in treated primary molars. Timepoint: 6 and 12 month after treatment. Method of measurement: Radiographic examination is performed to detect the presence or absence of internal resorbtion.;The frequency of occurrence of external resorbtion in radiographic images in treated primary molars. Timepoint: 6 and 12 month after treatment. Method of measurement: Radiographic examination is performed to detect the presence or absence of external resorbtion.;The frequency of occurrence of PDL widening in radiographic images i

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShirin Marzughi

Ilam University of Medical Sciences

shirin.marzoughi@gmail.com+98 84 3222 7134

Outcome results

None listed

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