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Endodontic Inflammation clinical trials

View clinical trials related to Endodontic Inflammation.

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NCT ID: NCT06176378 Completed - Clinical trials for Irreversible Pulpitis

A Clinical and Radiographic Evaluation of Low-Level Diode Laser Full Pulpotomy in Vital Permanent Teeth

Start date: October 12, 2020
Phase: N/A
Study type: Interventional

In this study, patients with symptoms of irreversible pulpitis in mature permanent molars were treated with two pulpotomies techniques after random allocation in either 2 groups: Diode laser pulpotomy and traditional pulpotomy using bioactive materials (retro mineral trioxide aggregate ) with each group.The null hypothesis of the study was there would be no difference in success rate between Diode laser and traditional methods of adult pulpotomy .

NCT ID: NCT04700995 Completed - Clinical trials for Apical Periodontitis

Postoperative Pain After Using NiTi Instruments

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

The aim of this randomized clinical trial was to compare the incidence, intensity and duration of postoperative pain following the removal of root canal obturation materials canals using rotary (ProTaper Universal or Hyflex EDM) or reciprocating file (Reciproc Blue or WaveOne Gold) systems. The null hypothesis tested was that there is no difference in postoperative pain following the retreatment procedure between the four systems used.

NCT ID: NCT04228913 Completed - Pain Clinical Trials

Effect of Different Obturation Techniques on Postoperative Pain

Start date: August 31, 2017
Phase: Phase 4
Study type: Interventional

This study evaluated the postoperative pain after the endodontic treatment by using three different obturation techniques. ( Cold lateral condensation (CLC), thermoplasticized solid-core carrier method (GuttaCore) and cold free-flow compation tecnique ( GuttaFlow2))

NCT ID: NCT04211519 Completed - Endodontic Disease Clinical Trials

Analysis of Bacterial Microbiome of Endodontically Infected Primary and Permanent Teeth

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Recognition of community profiles in endodontic infections may allow a better understanding of the pathogenesis of the disease and the establishment of more effective treatment protocols. Therefore, the aim of the present study was to investigate bacterial diversity in endodontically infected primary and permanent teeth using 16S rRNA gene sequencing and QIIME 2TM (Quantitative Insights Into Microbial Ecology 2) bioinformatics pipeline

NCT ID: NCT03802305 Completed - Clinical trials for Endodontic Inflammation

Comparison of Osteocentral Versus Locoregional Anesthesia in Case of Mandibular Molar Pulpitis

COQ
Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The irreversible acute pulpitis is the most common emergency at the hospital during dental consultation. Pulpitis are characterized by intense and spontaneous oro-facial pains. In case of mandibular molar, the emergency treatment consists in realizing a pulpotomy (eviction of cameral pulp) under locoregional anesthesia called inferior alveolar nerve block (IANB). The latter represents a real challenge, since inflammation may decrease its action. To mitigate this deficiency and the drawbacks of the IANB (onset and duration of the anesthesia, bites risk reported with IANB) other anesthesias are proposed. In particular the computerized intraosseous technique anesthesia of which the Quicksleeper™ system is a part. However, according to the observers, a mild to severe tachycardia have been reported. Very few valid clinical trials exists on the subject, most being realized with systems of intraosseous anesthesia other than Quicksleeper™. Therefore, the aim of this study is first to analyze the variations of the cardiovascular parameters into two groups of anesthesia: locoregional anesthesia and Quicksleeper ™ system; and then, to compare the efficiency, side effects, operating consequences of both techniques. This study should provide better data about potential risk with computerized intraosseous technique such has Quicksleeper ™ system in healthy or cardiovascular risk patient.

NCT ID: NCT03635515 Completed - Post-Operative Pain Clinical Trials

Occurrence of Post-op Pain Following Gentlewave

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

This is a clinical study that will investigate the occurrence of post-operative discomfort following the use of the Gentlewave System for root canal disinfection and irrigation. Assessment of discomfort level will be via a visualized analog pain scale.

NCT ID: NCT03551587 Completed - Clinical trials for Endodontic Inflammation

Comparison Between the Vibringe and the Conventional Needle

Start date: November 28, 2017
Phase: N/A
Study type: Interventional

The Vibringe is the first endodontic sonic irrigation system that enables delivery and activation of the irrigation solution in the root canal, in only one step. The activation of the disinfectant by acoustic streaming, enriches and completes the irrigation procedure and improves the success rate of endodontic treatments. It has been shown that this system significantly improves debridement. It also improves the disruption of the smear layer and biofilm by activating irrigation solutions. As there are no previous studies comparing the Vibringe system with other irrigation techniques under clinical settings, in this regard, the aim of this study is to evaluate whether irrigation with Vibringe provides more or less benefit in terms of postoperative pain when compared with the conventional needle technique.

NCT ID: NCT03472456 Completed - Clinical trials for Endodontic Inflammation

Endodontic Medications for Irreversible Pulpitis: Articaine or Eugenol?

Start date: March 22, 2018
Phase:
Study type: Observational

The objective of the study is to determine which of the two commonly used endodontic medications (Eugenol VS Articaine) is most effective in controlling postoperative pain in irreversible pulpitis of the mature permanent tooth in adults. To do so, an assessment of the pain felt by patients will be carried out a few days apart. The supposed results are that the medications are equivalent in terms of effectiveness on the pain, but could then present different economic arguments

NCT ID: NCT02437708 Completed - Clinical trials for Endodontic Inflammation

Regenerative Endodontic Procedure of Immature Permanent Teeth With L-PRF: a Pilot Controlled, Clinical Trial

Start date: September 2014
Phase: Phase 3
Study type: Interventional

This study evaluates the impact of autologous 'leucocyte and platelet rich fibrin' (L-PRF) on the periapical bone healing and further root development of infected immature permanent teeth. In the test group regenerative endodontic procedure (REP) is performed with L-PRF as scaffold, in the control group REP without L-PRF is performed .