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Pulpitis clinical trials

View clinical trials related to Pulpitis.

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NCT ID: NCT05622266 Recruiting - Clinical trials for Irreversible Pulpitis

Effectiveness of Pulpotomy in the Management of Mature Permanent Tooth With Irreversible Pulpits

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

This study is to evaluate the effectiveness of pulpotomy in mature permanent tooth with irreversible pulpits, and compare the clinical efficacy of pulpotomy and root canal therapy.

NCT ID: NCT05557812 Recruiting - Pulpitis Clinical Trials

A Clinical Trial Comparing FS With ZOE and Non-eugenol Based Materials in Primary Teeth Pulpotomies

Start date: February 2, 2023
Phase: Early Phase 1
Study type: Interventional

Internal resorption in the most common cause of failure in FS pulpotomies in primary molars. This has been attributed to the release of free eugenol from the zinc and eugenol mixture of the base material over the pulp tissue. Zinc oxide-eugenol (ZOE) paste is the most common base material placed over the infected pulp tissues during pulpotomies of primary molars, however the evidence suggests that the eugenol component has been associated with the failure of the vital pulp treatment in primary molars. Cavit (3M, US) is another base material that contains Zinc-oxide, zinc sulphate, and calcium salts without eugenol. The effectiveness of non-eugenol based Zinc oxide as a base material over ferric sulphate treated pulp has not been explored. The hypothesis is that the non-eugenol based ZOE could be used as an alternate to eugenol based ZOE and thereby avoid the radiological failures. Therefore, this randomized controlled clinical split-mouth trial aimed to evaluate and compare the effect of eugenol and non-eugenol based ZOE on the success of primary tooth pulpotomies where FS is used as a medicament.

NCT ID: NCT05427903 Recruiting - Pain, Procedural Clinical Trials

Two Approaches in Enhancing the Efficacy of Inferior Alveolar Nerve Block During Treatment of Mandibular First Permanent Molars With Symptomatic Irreversible Pulpitis

Start date: March 4, 2022
Phase: N/A
Study type: Interventional

The study is designed as a randomized parallel controlled trial with three groups. Participants aged above 18 years with the first permanent molars with symptomatic signs of irreversible pulpitis will be randomly assigned into 3 groups. The first group (experimental group) will be injected with 4% articaine 1:100.000 epinephrine (inferior alveolar nerve block) will be anesthetized using 4% articaine 1:100.000 plus cryotherapy application, and the second group (experimental group) will be anaesthetised with IANB plus buccal infiltration. For the third group (control group), the mandibular molars will be anaesthetized using epinephrine using the inferior alveolar nerve block.

NCT ID: NCT05406557 Recruiting - Clinical trials for Pulpitis - Irreversible

Partial Versus Miniature Pulpotomy in Teeth With Irreversible Pulpitis

Start date: May 12, 2022
Phase: N/A
Study type: Interventional

This study will compare the outcome of partial and miniature pulpotomy in mature permanent molars with symptomatic partial irreversible pulpitis

NCT ID: NCT05402098 Recruiting - Clinical trials for Pulpitis - Irreversible

Outcome Following Endodontic Treatment Using Traditional Access Versus Conservative Access

Start date: May 12, 2022
Phase: N/A
Study type: Interventional

This study will compare the outcome of endodontic treatment using conservative or traditional access design in permanent molars with clinical signs indicative of irreversible pulpitis

NCT ID: NCT05338671 Recruiting - Post Operative Pain Clinical Trials

Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment

Start date: September 29, 2021
Phase: Phase 4
Study type: Interventional

This study will assess the efficacy of two local anesthetics (2% lidocaine 1:100,000 epinephrine and 0.5% bupivicaine 1:200,000 epinephrine) in reducing post-operative pain in patients receiving endodontic treatment.

NCT ID: NCT05336682 Recruiting - Clinical trials for Pulpitis - Irreversible

Evaluation of Lesion Sterilization and Tissue Repair Techniques Versus Pulpectomy in Primary Molars With Inflammed Pulp

Start date: September 20, 2022
Phase: N/A
Study type: Interventional

Group I (Experimental group I): Lesion Sterilization and Tissue Repair with radicular instrumentation. Coronal and accessible radicular pulp tissue are extirpated using rotary files. After proper drying, the paste is placed in the cavity and canals. Group II (Experimental group II): Lesion Sterilization and Tissue Repair with no radicular instrumentation. Only the coronal pulp is removed, the pulpal floor is covered with triple antibiotic paste with propylene glycol mix. Group III (Control group): Conventional pulpectomy. Pulp tissue extirpation is done. Biomechanical preparation is done using rotary files with frequent irrigation with Chlorhexidine. The canals are dried using sterile absorbent paper points followed by obturation by the paste of Zinc oxide and eugenol.

NCT ID: NCT05279820 Recruiting - Clinical trials for Irreversible Pulpitis

Comparative Study of the Outcome of Partial and Full Pulpotomy in Irreversible Pulpits

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

This study aims at comparing the outcome of partial pulpotomy and full pulpotomy in the management of carious pulp exposures in permanent teeth with a clinical diagnosis of irreversible pulpits. The primary outcome is resolution of symptoms and the secondary outcome is clinical and radiographic normality at 1 and 2 years follow up. The study design will be a double blind randomized clinical trial.

NCT ID: NCT05279781 Recruiting - Caries Clinical Trials

Outcome of Pulpotomy Versus Root Canal Therapy

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

Root canal therapy (RCT) is indicated once the pulp is diagnosed with irreversible pulpitis. Despite favorable success rate reported for RCT in vital cases, it is time consuming, and might increases fracture susceptibility of teeth. With the advancement of materials and better understanding of pulpal healing, vital pulp therapy is practiced as an alternative treatment with high success rate. The aim of this study is to explore the outcome, quality of life and patient satisfaction after full pulpotomy compared to RCT.

NCT ID: NCT05190406 Recruiting - Clinical trials for Irreversible Pulpitis

Success and Quality of Life Following Complete Pulpotomy and Root Canal Treatment

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the Success and quality of life following complete pulpotomy and root canal treatment in teeth with clinical signs indicative of irreversible pulpitis.