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Pulpitis clinical trials

View clinical trials related to Pulpitis.

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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: NCT03415724 Not yet recruiting - Clinical trials for Irreversible Pulpitis

Comparison of Anesthetic Efficacy of Dexmedetomidine and Epinephrine With Lidocaine in Irreversible Pulpitis

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

Aim of the study is to determine and compare the anaesthetic efficacy of dexmedetomidine and epinephrine in combination with 2% lidocaine for inferior nerve block in patients with irreversible pulpitis. Study will be conducted in Post Graduate Institute of Dental Sciences, Rohtak in department of Conservative Dentistry & Endodontics. Vital mature permanent mandibular molars with radiographically exposed dentinal caries and with signs of irreversible pulpitis will be included in the study. The patients will be randomly allocated into two control and two experimental groups and nerve block will be given according to standard protocol.

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.

NCT ID: NCT03410212 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

Efficacy of Block Injection of an Anti Inflammatory Medicine in Patients With Mandibular Dental Pain

IANB
Start date: February 15, 2018
Phase: Phase 2
Study type: Interventional

The aim of this study is to determine whether inferior alveolar nerve block of ketorolac and lidocaine would improve the success rate in teeth with symptomatic irreversible Pulpitis. Design: In this randomized double-blind clinical trial, sixty healthy adult volunteers with including criteria have been randomly divided into two groups (n=30). Following the 5 minutes of the first IANB using 1.8 ml 2% lidocaine 2% containing 1:100000, the patients of case group have received a standard inferior alveolar nerve block injection that used 1 ml ketorolac tromethamine 30 mg/ml. The patients of the control group received a sham injection. After achieving the lip numbness, access preparation initiated after 15 minutes of initial IANB with two negative responses to the electric pulp test. Any pain during caries and dentin removal, access cavity preparation, and root canal preparation have been recorded using analog visual scale (HP-VAS). The success was considered as none or mild pain during treatment. The data have been analyzed using Mann-U-Whitney test. Intervention main outcome measures: Pain during caries and dentin removal access cavity preparation, and root canal preparation using VAS.

NCT ID: NCT03341260 Completed - Clinical trials for Pulpitis - Irreversible

Effect of Preoperative Diclofenac Potassium on Postoperative Endodontic Pain

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

The purpose of this study is to assess the effect of preoperative a single-dose of 50 mg diclofenac potassium on postoperative endodontic pain in mandibular molars with symptomatic irreversible pulpitis.

NCT ID: NCT03339544 Not yet recruiting - Pulpitis Clinical Trials

Celebrex Premedication in Teeth With Symptomatic Irreversible Pulpitis

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

Assessing the efficacy of Celebrex premedication on pain during and after endodontic treatment in teeth with symptomatic irreversible pulpits

NCT ID: NCT03335007 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

Pretreatment Aceclofenac Effect on Pain and Analgesic Intake After Endodontic Treatment

Start date: May 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this prospective, randomized, double-blind, clinical trial is to evaluate the effect of a preoperative, single, oral dose of aceclofenac (100 mg) on postendodontic pain at 6, 24 and 48 hours, postoperative pain at injection area at 6, 24 and 48 hours and analgesic intake after single-visit root canal treatment.

NCT ID: NCT03286959 Completed - Reversible Pulpitis Clinical Trials

Effect of Liners on Pulpal Outcome and Restoration Survival After Partial Caries Excavation

Start date: November 6, 2016
Phase: N/A
Study type: Interventional

Aim of the study was to determine the effectiveness of cavity liners regarding survival of restoration beneath composite restoration after partial caries removal in permanent teeth with deep caries and to evaluate and compare the pulp vitality outcome both clinically and radiologically with and without liners. Study was conducted in Post Graduate Institute of Dental Sciences, Rohtak in department of Conservative Dentistry & Endodontics. Mature permanent mandibular molars with deep dentinal caries and without any signs of irreversible pulpitis were included in the study. After partial excavation of caries, patients were randomly allocated into three groups- RMGIC, CH and DIRECT COMPOSITE group and were restored according to standard protocol.

NCT ID: NCT03284697 Completed - Reversible Pulpitis Clinical Trials

Direct Pulp Capping With MTA and Calcium Hydroxide.

Start date: October 14, 2016
Phase: N/A
Study type: Interventional

Aim of the study was to evaluate and compare clinical and radiographic success with MTA and calcium hydroxide as direct pulp capping materials in cariously exposed mandibular molars. Study was conducted in Post Graduate Institute of Dental Sciences, Rohtak in department of Conservative Dentistry & Endodontics. Mature permanent mandibular molars with reversible pulpitis exhibiting occlusal pulp exposure from primary dental caries were included in the study. After excavation of caries and obtaining pulpal hemostasis, patients were randomly allocated into two groups- MTA and Calcium Hydroxide. Pulp was capped with respective allocated material and then tooth in both groups were restored according to standard protocol.