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Pulpitis clinical trials

View clinical trials related to Pulpitis.

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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: NCT03749408 Completed - Clinical trials for Irreversible Pulpitis

Effect of Addition of Mannitol to Bupivacaine on IANB Success and Post-endodontic Pain

Start date: December 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Inferior alveolar nerve block using either 0.5% bupivacaine alone or in addittion to mannitol in patients with irreversible pulpitis in mandibular molars.

NCT ID: NCT03708081 Completed - Pulpitis Clinical Trials

Comparative Evaluation of Different File Systems in Postoperative Pain

Start date: June 1, 2017
Phase:
Study type: Observational [Patient Registry]

Postoperative pain is a frequent complication associated with root canal treatment. The apical extrusion of irrigant and debris, including bacteria and necrotic tissue, may lead to postoperative pain, periapical inflammation, and flare-ups. The instrumentation technique and the file design may affect the amount of debris extrusion. The aim of this study was to evaluate the influence of instrumentation techniques on the incidence and intensity of postoperative pain after single-visit root canal treatment.

NCT ID: NCT03692039 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

Comparison Between M-Pro and ProTaper Next

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

Comparing the postoperative pain resulting after mechanical instrumentation using M-pro files versus that resulting after using ProTaper Next rotary files in lower molar with symptomatic Irreversible pulpitis molars.

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: NCT03553641 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

The Effect of Central Sensitization on Assessment Capacity of Patients

Start date: November 1, 2017
Phase:
Study type: Observational [Patient Registry]

the aim of this study is to evaluate the effect of dental hyperalgesia and mechanical allodynia on the assessment capacity of individuals in a local Turkish population. The hypothesis of this study is that excessive amounts of pain and a major functional shift in the somatosensory system due to central sensitization might cause unwitting intent.

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: NCT03490422 Completed - Pulpitis Clinical Trials

Pulpotomy in Carious Permanent Mature Teeth: Pulp Survival and Risk Factors

Start date: October 2013
Phase: N/A
Study type: Interventional

This Trial evaluated the extent of pulp survival following pulpotomy in the permanent tooth pulp exposed by caries and identify potential risk factors for pulpal complications.

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: NCT03412318 Completed - Acute Pulpitis Clinical Trials

Evaluation of the Effect of Root Canal Preparation by TF and M-Pro on Post-Operative Pain After Single Visit Endodontic Treatment

Start date: October 6, 2018
Phase: N/A
Study type: Interventional

A study to comparatively evaluate the post operative pain between root canal preparation by reciprocating file (TF) and full rotation file (M-Pro) in patients with single rooted teeth with acute irreversible pulpits.