Clinical and Radiographic Assessment of Bio C Repair, Biodentine and Mineral Trioxide Aggregate

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-10
SponsorCairo University

About this trial

The aim of this study is to assess Clinical and Radiographical effect of Bio C repair, Biodentine and Mineral Trioxide Aggregate when used as pulpotomy Agents in Immature Permanent Molars with Pulpits.

Eligibility criteria

Qualifiers

Children aged 6-10 years with asymptomatic/symptomatic disease and having vital immature permanent posterior teeth with clinical exposure to dental caries of the pulp and bleeding.

Posterior teeth had deep caries with pulp exposure.

Posterior teeth that exhibited preoperative symptoms, such as referred pain, spontaneous pain or pain induced during thermal and cold sensitivity tests, with a range of symptoms that can last from seconds to hours compared to the control teeth.

Posterior teeth without prominent radiolucency in the furcation or periapical regions.

Disqualifiers

• (1) Patients with contraindications of the to-be-performed dental treatment.

(2) Teeth with completed VPT or RCT.

(3) Teeth with furcation, prominent radiolucency in the periapical regions, or external or internal resorption.

(4) Teeth with pulpitis attributed to tooth fracture, cracking, periodontitis or wedge-shaped defects.

Trial design

Treatments tested in this trial

  • Biodentine
  • Bio C repair

Treatment groups

60 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators