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Dental Pulp Exposure clinical trials

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NCT ID: NCT06402032 Completed - Clinical trials for Pulp Exposure, Dental

Clinical and Histological Evaluation of Hesperidin as a Direct Pulp Capping Material

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

Direct pulp capping technique is one of the oldest known treatments for exposed pulp tissue, and there is a continuous requirement for the most efficient materials to be used in this approach. Successful pulp capping is the usual way to preserve the vitality of tooth and avoid root canal treatment or surgical tooth extraction.

NCT ID: NCT04989036 Completed - Clinical trials for Pulp Exposure, Dental

Biodentine Vital Pulpotomy in Immature Molars

Start date: October 1, 2016
Phase: Phase 4
Study type: Interventional

This study aimed to evaluate the clinical and radiographic success of pulpotomy in cariously exposed vital immature first permanent molars using calcium hydroxide and calcium silicate-based material (Biodentine ™). After a 12 months postoperative period, Biodentine ™ proved very useful as a successful pulpotomy agent in young permanent teeth.

NCT ID: NCT03838068 Completed - Clinical trials for Pulp Exposure, Dental

Pulpotomy Technique Preserving Vitality of Traumatized Anterior Permanent Immature Teeth

Start date: January 18, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Aim of the study: To compare the clinical and radiographic outcomes of mineral trioxide aggregate (MTA) and Biodentine as vital pulp therapy materials (pulpotomy) preserving the vitality of traumatized immature anterior permanent teeth. Materials and Methods: fifty vital traumatized immature anterior permanent teeth exposed with symptomatic /asymptomatic pulpitis were included in the study according to inclusion criteria and were equally divided in two groups. Included teeth were randomly assigned to either a control group (MTA 25 teeth) or a test group (Biodentine 25 teeth). After conducting pulpotomy and covering pulp stumps with the MTA and Biodentine, treated teeth received permanent restorations. Blinded clinical and radiographic evaluations were performed at different time intervals (base line immediate postoperative, 6, 12 and 18 months) according to clinical and radiographic criteria of success. Data were recorded and analyzed.

NCT ID: NCT03631511 Completed - Clinical trials for Dental Pulp Exposure

Histological Evaluation of Hard Tissue Formation After Direct Pulp Capping With RetroMTA

RetroMTA
Start date: April 3, 2016
Phase: N/A
Study type: Interventional

This study presents a clinical and histological evaluation of human pulp tissue responses after direct capping using RetroMTA. Seven teeth were subjected to pulp exposure, direct capping with RetroMTA, and restoration with a composite resin. Seven months later, the teeth were clinically and radiographically evaluated. The teeth were then extracted and subjected to histological processing and evaluation.

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: NCT02789423 Completed - Clinical trials for Dental Pulp Exposure

Clinical & Radiographical Evaluation of the Effect of Dycal & Biodentine in DPC in Primary Teeth

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

The purpose of this study was clinical and radiographical evaluation of the effect of calcium hydroxide cement (Dycal) and calcium silicate cement (Biodentine) in direct pulp capping in primary teeth.

NCT ID: NCT02487329 Completed - Clinical trials for Dental Pulp Exposure

The Effect of Laser Combined With Pulp-capping Agents on Direct Pulp Capping

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this randomized clinical study was to evaluate the efficiency of Er,Cr:YSGG laser irradiation combined with a resin based tricalcium silicate material and calcium hydroxide (CH) in direct pulp capping for 3 months follow-up period.Sixty permanent vital teeth without symptoms and radiographic changes were randomly assigned to 4 groups (n=15): Gr 1: The exposed area was sealed with CH paste, Gr 2: The treated area was sealed with CH paste following Er,Cr:YSGG laser irradiation at an energy level of 0,5 W without water and 45% air, Gr 3: Resin based tricalcium silicate material (TheraCal LC) was applied directly to the exposed pulp, Gr 4: TheraCal LC was applied following irradiation with Er,Cr:YSGG laser.

NCT ID: NCT02019563 Completed - Dental Caries Clinical Trials

MTA/FS Pulpotomy for Vital Primary Incisors: A Randomized Controlled Trial

MTA/FS
Start date: September 2010
Phase: Phase 2
Study type: Interventional

To compare radiographic and clinical outcomes and survival of mineral trioxide aggregate/ferric sulfate (MTA/FS) pulpotomy and root canal therapy (RCT) in carious vital primary maxillary incisors.

NCT ID: NCT01468480 Completed - Clinical trials for Dental Pulp Exposure

Human Pulpal Response After Pulp Capping With Four Different Agents

Start date: June 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Application of four different pulp capping methods on human sound premolars after intentional exposure of the buccal pulp horn through a class one occlusal cavity.

NCT ID: NCT00812877 Completed - Clinical trials for Dental Pulp Exposure

Pulp Capping With Two Different Agents

MTA
Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if MTA or calcium hydroxide are more effective as pulp capping agents