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Effect of Direct Pulp Capping with Propolis and Calcium Hydroxide versus Mineral Trioxide Aggregate on Formation of Dentin Bridge in patents who are candidate for extraction of the third molar

Effect of Direct Pulp Capping with Propolis and Calcium Hydroxide versus Mineral Trioxide Aggregate on Formation of Dentin Bridge in patents who are candidate for extraction of the third molar: a double blinded randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201403049014N30
Enrollment
45
Registered
2014-03-11
Start date
2014-04-09
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

Formation of dentin bridge. Abnormal hard tissue formation in pulp

Interventions

Intervention 1: Direct pulp capping of the third molar with propolis at 3 to 3.5 mm in depth, 4 to 4.5 mm width mesiodistally, and 3 to 3.5 mm width buccolingually. Intervention 2: Direct pulp capping
Treatment - Drugs
Treatment - Other
Direct pulp capping of the third molar with propolis at 3 to 3.5 mm in depth, 4 to 4.5 mm width mesiodistally, and 3 to 3.5 mm width buccolingually
Direct pulp capping of the third molar with calcium hydroxide at 3 to 3.5 mm in depth, 4 to 4.5 mm width mesiodistally, and 3 to 3.5 mm width buccolingually
Direct pulp capping of the third molar with mineral trioxide aggregate at 3 to 3.5 mm in depth, 4 to 4.5 mm width mesiodistally, and 3 to 3.5 mm width buccolingually

Sponsors

Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (a) candidate for extraction of the third molar; (b) age of 20 to 30 years. Exclusion criteria: (a) presence of and dental caries in the third molar; (b) history of trauma to the third molar; (c) presence of lesion in periapical or periodontal area.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Formation of dentin bridge. Timepoint: 45 days after intervention. Method of measurement: through assessing the third molar histologically.

Secondary

MeasureTime frame
Presence of inflammation. Timepoint: 45 days after intervention. Method of measurement: through assessing the third molar pulp histologically.;Quality of the dentin bridge. Timepoint: 45 days after intervention. Method of measurement: through assessing the third molar histologically.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Golsa Salehi Mehr

School of Dentistry

g.salehi@umsha.ac.ir+98 81 1838 1086

Outcome results

None listed

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