Skip to content

Comparison of the clinical and radiographic effect of Endoseal MTA and MTA in pulpotomy treatment of primary teeth

Comparison of the clinical and radiographic effect of Endoseal MTA and MTA in pulpotomy treatment of primary teeth

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171013036741N2
Enrollment
45
Registered
2025-02-14
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Diseases related to the pulp of primary teeth. Pulpitis

Interventions

Intervention 1: Intervention group: MTA (Angelus, Londrina, PR, Brazil) It is prepared with the consistency of sand-like and according to the manufacturer's recommendation, and it is placed on the too

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 8 Years

Inclusion criteria

Inclusion criteria: Healthy and not taking antibiotics in the previous 14 days Cooperative (Frankel 3 and 4) Having at least two asymptomatic carious primary molars with the possibility of pulp exposure

Exclusion criteria

Exclusion criteria: Spontaneous pain Soft tissue swelling and fistula mobility pain on percussion internal and external resorption in radiography pulp degeneration and calcification Physiological analysis of more than 1/3 of root

Design outcomes

Primary

MeasureTime frame
Clinical condition of the tooth. Timepoint: 3 and 6 months after therapeutic intervention. Method of measurement: The clinical signs are examined and recorded by a professor specializing in pediatric dentistry. The radiographic symptoms are checked by the same professor after preparing a periapical photograph and comparing it with the baseline photograph (immediately after treatment). Clinical and radiographic evaluation is based on the modified ZURN AND SEALE criteria. Clinical: no symptoms / minor discomfort / mild discomfort / high discomfort | Radiography: no symptoms / analysis and internal changes of teeth / analysis and external changes of teeth / bone loss.;Toothache. Timepoint: 3 and 6 months after therapeutic intervention. Method of measurement: Pain is registered through a self-reported index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRosa Haghgoo

Shahed University

haghgoodent@yahoo.com+98 21 8895 9210

Outcome results

None listed

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