Evaluatıon of the Effect of Pulpotomy Treatments Wıth Dıfferent Bıomaterıals on Postoperatıve Paın In Permanent Molars

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-65
SponsorTC Erciyes University

About this trial

The aim of this study was to evaluate the results of partial and total pulpotomy with mineral trioxide aggregate (BIO MTA+) and bioceramic sealer (Well Root PT) in terms of pain and vitality in permanent molars with exposed pulp due to caries.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients over 18 years of age with no significant health problems.

Restorable and periodontally healthy teeth.

Teeth with complete root development.

Teeth with cold sensitivity and positive response to electric pulp testing.

Disqualifiers

Patients with systemic diseases or allergic reactions

Teeth with open apex

Carious teeth that do not respond to pulp sensitivity tests

Teeth without signs of bleeding after opening the pulp chamber.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Treatment as usual

    Drug

    Well-Root PT is clinically used in many areas such as pulp capping, perforation and resorption repair, root tip filling and apexification. As Well-Root PT is available in pre-mixed capsule form, it can provide a consistent and adequate consistency and clinical convenience. Well-Root PT can be applied directly into the oral cavity by placing the capsule in a syringe. In addition, Well-Root PT has a shorter setting time than MTA.Despite these advantages, there is no study in the literature on the effect of Well-Root PT on postoperative pain and tooth vitality after pulpotomy in mature permanent molars

Treatment groups

54 Participants
are divided into 2 treatment groups
Group A: BİO MTA+ (CERKAMED, Poland) groupExperimental treatment 1 intervention
Group B: Well-Root PT (Vericom Co., Chuncheon, Kore) groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

assessment of postoperative pain with questionnaires

Visual Analogue Scala (VAS) will be used . 0: no pain 100: Worst pain

Time frame
12 month

Secondary outcomes

Other outcomes

Sponsors and contacts

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