Comparison of clinical and radiographic success rate of pulpotomy in primary molars using Biodentine, Endo repair and Formocresol: A double blind randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180521039763N2

Enrollment

105

Registered

2019-05-09

Start date

2018-10-22

Completion date

Unknown

Last updated

2019-05-21

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

Conditions

Pulpitis.

Interventions

Intervention 1: Control group: Cotton pellet impregnated with formocresol (sultan, USA) is placed on the pulp for 5 minutes. Intervention 2: Intervention group: 1: After pulp tissue homeostasis, the B

Eligibility

Sex/Gender

All

Age

3 Years to 10 Years

Inclusion criteria

Inclusion criteria: Pulp exposure due to caries No pathologic mobility No history of spontaneous pain No sinus tracts, abscess or swelling Restorable teeth with ssc Hemostasis could be easily achievable No internal or pathologic external root resorption No interradicular or periapical radiolucency

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Mutation and cytogenetic formocresol. Timepoint: 0 , 6 and 12 months later. Method of measurement: Through clinical and radiographic evaluation and questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzane Jalali

Kerman University of Medical Sciences

fznjalali@gmail.com+98 34 3211 9021

Outcome results

None listed

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