Coldceramic in primary Tooth Pulpotomy

Evaluation and comparison of the effectiveness of mineral trioxide aggregate and cold ceramic in the success of primary molars pulpotomy: a clinical and radiographic study

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220426054664N1

Enrollment

Registered

2022-05-31

Start date

2022-06-10

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

pulpotomy.

Interventions

Intervention 1: Intervention group: Treatment of primary molar pulpotomy with cold ceramic , which is made in Iran and contains compounds of calcium oxide, silicon acid, these compounds are 93% of its

Eligibility

Sex/Gender

All

Age

4 Years to 9 Years

Inclusion criteria

Inclusion criteria: General and mental health of the child Lack of clinical adverse symptoms in the target tooth such as spontaneous pain or nocturnal pain, swelling of pulpal origin, pathological sagging, fistula Lack of adverse radiographic signs of the desired tooth such as internal root resorption, external root resorption and periapical or furca area

Exclusion criteria

Exclusion criteria: Failure to refer the patient for 3 and 6 month follow-up Having an underlying disease

Design outcomes

Primary

Measure	Time frame
Success of pulpotomy treatment. Timepoint: Follow-up 3 and 6 months after treatment. Method of measurement: Radiographs and clinical examination.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBita Rasteh

Ahvaz University of Medical Sciences

bitarasteh99@gmail.com+98 61 4352 4848

Outcome results

None listed

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