BiodentineTM Versus Formocresol Pulpotomy Technique in Primary Molars

PHASE4CompletedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

May 31, 2014

Primary Completion Date

December 31, 2015

Study Completion Date

September 30, 2016

Conditions
Dental CariesPulpotomy
Interventions
OTHER

BiodentineTM

In the experimental group, BiodentineTM was used following the manufacturer's recommendations. The whole pulp chamber was entirely filled with BiodentineTM until the occlusal surface. Follow-up was done for all children clinically at 3, 6 and 12 months and radiographically at 6 and 12 months.

DRUG

Formocresol

In control group, a sterile cotton pellet moistened with 1:5 concentration formocresol then blotted to remove excess was placed for 5 minutes on the pulp stumps and then the pulps were covered with zinc oxide-eugenol (IRM; Dentsply, Milford, DE) dressing. Follow-up was done for all children clinically at 3, 6 and 12 months and radiographically at 6 and 12 months.

Trial Locations (1)

21589

King Abdulaziz University, Faculty of Dentistry, Jeddah

All Listed Sponsors
lead

King Abdulaziz University

OTHER

NCT03779698 - BiodentineTM Versus Formocresol Pulpotomy Technique in Primary Molars | Biotech Hunter | Biotech Hunter