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Pulpitis clinical trials

View clinical trials related to Pulpitis.

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NCT ID: NCT03189771 Not yet recruiting - Clinical trials for Apical Periodontitis

Effect of Occlusal Reduction on Post-operative Pain

Start date: June 27, 2017
Phase: N/A
Study type: Interventional

effect of occlusal reduction on post-operative pain is evaluated after single visit root canal treatment in upper and lower molar teeth in patients with sypmtomatic irreversible pulpitis and apical periondontis

NCT ID: NCT03186690 Active, not recruiting - Clinical trials for Irreversible Pulpitis

Similar Outcomes of Vital Pulp Therapy Using Mineral Trioxide Aggregate or Biodentine™

Start date: July 4, 2013
Phase: N/A
Study type: Interventional

This study aimed to evaluate the clinical performance of White MTA (MTA, Angelus, Londrina, Brazil) and Biodentine™ in pulp capping of cariously exposed mature permanent teeth. The investigator performed a prospective longitudinal randomized controlled study utilizing vital permanent mature teeth with deep caries. Patients will be divided randomly into Biodentine™ and MTA groups; Teeth will be assessed clinically and radiographically prior to the procedure. Caries will be excavated under local anesthesia, hemostasis is achieved after pulp exposure using NaOCl and will be capped with Biodentine™ or MTA. Clinical and radiographical follow-up will be performed by a blinded calibrated evaluator after six months and one year, and yearly after.

NCT ID: NCT03174860 Completed - Anesthesia, Local Clinical Trials

Effect of Preoperative Diclofenac Potassium on Articaine Buccal Infitration Success

Start date: October 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to assess the effect of preoperative Diclofenac Potassium (50 mg Cataflam) on the anesthetic success of buccal infiltration with 4% articaine with epinephrine 1:200,000 in mandibular molars with symptomatic irreversible pulpitis.

NCT ID: NCT03168620 Completed - Pulpitis Clinical Trials

Effect of Glass Ionomer Cement as an Interim Restoration in Diagnosis of Pulpal Status

Start date: May 20, 2015
Phase: N/A
Study type: Interventional

Aim: To evaluate whether glass ionomer interim therapeutic restoration (ITR) in asymptomatic teeth with deep cavities can help in determining the pulp status. Methodology: 146 mandibular molars with deep carious lesion having positive response to pulp sensitivity were randomly allocated to two study groups (75-ITR, 71- NON-ITR group). In the first group after partial caries removal(PCR), interim therapeutic restoration of glass ionomer cement (GIC) Ketac molar was placed for one month before definitive adhesive restoration. In NON-ITR group, cavity preparation was similar to ITR group, but definitive restoration was done in the same visit. Two examiners evaluated the clinical and radiographic outcomes for 18 months. Success was defined as absence of signs and symptoms of irreversible pulpitis and absence of periapical alterations.

NCT ID: NCT03163420 Active, not recruiting - Clinical trials for Irreversible Pulpitis

Diclofenac Potassium on IANB Efficacy in Symptomatic Irreversible Pulpitis

Start date: July 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this clinical trial is to evaluate the effect of pre-operative administration of diclofenac potassium on the efficacy of inferior alveolar nerve block on using 2% mepivacaine anaesthetic agent in patients with symptomatic irreversible pulpitis.

NCT ID: NCT03146481 Completed - Clinical trials for Irreversible Pulpitis

Pre-operative Aceclofenac on the Anesthetic Efficacy of IANB in Symptomatic Irreversible Pulpitis

Start date: July 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this randomized, double-blinded, controlled study is to evaluate the effect of pre-operative oral aceclofenac on the success of the inferior alveolar nerve block with 2% Mepivacaine containing 100,000 Epinephrine for patients with symptomatic irreversible pulpitis.

NCT ID: NCT03117491 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

Effect of Inferior Alveolar and Gow-Gates Nerve Block Techniques for Symptomatic Mandibular Molars

Start date: December 1, 2015
Phase: Phase 3
Study type: Interventional

Introduction: to evaluate the efficacy of inferior alveolar nerve block (IANB), Gow-Gates nerve block (GGNB), and their combination in patients with irreversible pulpitis. Methods: One hundred fifty subjects with irreversible pulpitis of a mandibular molar were selected. subjects randomly received two IANB injections or two GGNB injections or their combination of 1.8 mL 2% lidocaine with 1:100,000 epinephrine. Success was specified as no or mild pain on the basis of Heft-Parker visual analogue scale recordings up on the access cavity preparation or initial instrumentation. Data were analyzed by Kruskal-Wallis, and ANOVA tests.

NCT ID: NCT03116672 Completed - Clinical trials for Pulpitis - Irreversible

The Outcome of Preoperative Administration of Single-dose Ketorolac, Non-steroidal Anti-inflammatory Drug and Placebo

PreOp
Start date: February 2, 2016
Phase: N/A
Study type: Interventional

Aim. To compare the outcome of preoperative administration of single-dose ketorolac, non-steroidal anti-inflammatory drug and placebo on postoperative pain in teeth with irreversible pulpitis and apical periodontitis.

NCT ID: NCT03096587 Recruiting - Clinical trials for Symptomatic Irreversible Pulpitis

Effect Of XP Endo Finisher Versus Ultrasonic Activated Irrigation On Post-operative Pain In Endodontic Treatment of Symptomatic Irreversible Pulpitis

RCT
Start date: April 15, 2017
Phase: N/A
Study type: Interventional

Recruited patients with symptomatic irreversible pulpitis are assigned to interventional (XP Endo Finisher file) and control group(ultrasonic activated irrigation) to undergo single visit endodontic treatment and record postoperative pain afterwards.

NCT ID: NCT03071588 Active, not recruiting - Reversible Pulpitis Clinical Trials

Assessment of a New Protocol for Indirect Pulp Capping Procedures

Start date: July 2014
Phase: N/A
Study type: Interventional

The aim of the study is to assess clinically, radiographically and microbiologically a new protocol for indirect pulp capping procedures compared to the conventional protocol in painful teeth. It was postulated that there is no difference between both protocols in terms clinical, radiographical and microbial outcome measure after one year of follow up in painful teeth.