sodium hypochelorite pulpotomy success in primary molars

comparison of success rate of ferric sulfate and sodium hypochlorite for primary molar teeth pulpotomy in 5-8 years children .

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2012100711028N1

Enrollment

Registered

2013-05-20

Start date

2013-05-12

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

pulpitis. Pulpitis

Interventions

Intervention 1: intervention group: after pulpotomy, sodium hypochlorite is placed into the pulp chamber as the drug for30 second. Intervention 2: Control Group: after pulpotomy, ferric sulfate is pl

Treatment - Drugs

intervention group: after pulpotomy, sodium hypochlorite is placed into the pulp chamber as the drug for30 second

Control Group: after pulpotomy, ferric sulfate is placed into the pulp chamber as the drug for15 second.

Eligibility

Sex/Gender

All

Age

5 Years to 8 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Children 5-8 years old; presence of at least 2 primary second molars teeth in mandible requiring pulpotomy. Exclusion criteria:Children over 8 years; Absence of two primary second molars in mandible; pulpotomy contraindications of primary molars including: nocturnal pain; presence of fistulas; abscesses, internal and external root resorption; periapical lucency; furcal lucency; Continous bleeding after removing the pulp and placed dry cotton for 5 minutes;teeth wich will show phisyologic mobility or exfuliated in 6 or 12 months fallow up.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

Measure	Time frame
External resorbtion. Timepoint: Baseline, 6 months after the intervention, and 12 months after intervention. Method of measurement: radiography.;Furcal radiolucency. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: radiography.	—

Primary

Measure	Time frame
Internal resorption. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: radiography.;Dental abscess and fistula. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: clinical examination.;Periapical radiolucency. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: radiography.;Pain. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: clinical examination and questions.	—

Measure

Time frame

Internal resorption. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: radiography.;Dental abscess and fistula. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: clinical examination.;Periapical radiolucency. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: radiography.;Pain. Timepoint: 6 months after the intervention, and 12 months after intervention. Method of measurement: clinical examination and questions.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Dehghan

Islamic Azad University Khorasgan Branch

za.dehghan@khuisf.ac.ir+98 31 1673 3103

Outcome results

None listed

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