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Dental Pulp Necrosis clinical trials

View clinical trials related to Dental Pulp Necrosis.

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NCT ID: NCT01212939 Terminated - Infection Clinical Trials

Revitalization of Teeth With Necrotic Pulps and Open Apexes Using Platelet-Rich Plasma

Start date: October 2012
Phase: N/A
Study type: Observational

When root canals of infected teeth with closed ends are cleaned, disinfected and filled, the results are predictable with excellent outcomes. However, in a tooth with incomplete root development, the end of the root(s) must be closed before filling the root canals. One or two-step artificial barrier using mineral trioxide aggregate (MTA) has been used before filling the root canals of these teeth. Despite the high success of this treatment, this procedure does not result in complete root formation and these teeth are susceptible to root fracture. A number of case reports in scientific journal have shown the possibility for regeneration of nerve within the root canal space and continued root development in teeth with dead nerves and open ends. There is very little information regarding the use of stem cells and growth factors from the blood of patients to regenerate the nerves in these teeth. Platelet rich plasma (PRP) from whole blood has been mentioned in the literature as a potential ideal material for regeneration of nerves in these teeth. The purpose of this study is to investigate the use of PRP to regenerate tooth nerve and close the root ends in teeth with root canal infection and open root ends.

NCT ID: NCT00881907 Completed - Pulp Necrosis Clinical Trials

Tissue Characterization in Teeth Treated With a Regeneration Protocol

Start date: March 2010
Phase: Phase 0
Study type: Interventional

The purpose of the investigators study is to characterize the composition of the hard and soft tissues present in root canals of teeth previously diagnosed with necrotic pulps and incomplete root formation and treated with a triple antibiotic regeneration protocol. The investigators hypothesis is that treatment of teeth with necrotic pulps and immature apices with triple antibiotic paste will stimulate continued root formation by the deposition of dentin at the root apices. The primary outcome measure will be histological identification of mineralized tissue and adherent cells in the apical third of these teeth.

NCT ID: NCT00881491 Completed - Pulp Necrosis Clinical Trials

Treatment Outcome With a Revascularization Protocol Using the Triple Versus Double Antibiotic Paste

Start date: April 2009
Phase: Phase 0
Study type: Interventional

The purpose of this study is to determine the treatment outcomes in permanent teeth with necrotic pulp and immature root development that undergo a regenerative procedure using a triple antibiotic paste (ciprofloxacin, metronidazole, minocycline) versus a double antibiotic paste (ciprofloxacin, metronidazole)compared to the commonly used mineral trioxide aggregate (MTA) apexification treatment.

NCT ID: NCT00624572 Active, not recruiting - Clinical trials for Dental Pulp Necrosis

Efficacy of Chlorexidine as Intracanal Medicament in Primary Teeth

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the action of the chlorexidine as intracanal medicament in the reduction of the levels of bacteria inside root canals of primary molar teeth with pulpal necrosis.

NCT ID: NCT00472173 Completed - Clinical trials for Dental Pulp Necrosis

Assessment of a New Apexification Method for Patients Presenting a Non Vital Immature Tooth

APEXMTA
Start date: May 2007
Phase: Phase 3
Study type: Interventional

Pulp necrosis is one of the main complication of dental trauma. When it happens on an immature tooth, pulp necrosis implies a lack of root maturation and apical closure. A therapy called apexification is required to induce the formation of a calcified apical barrier allowing a permanent and hermetic root filling.The aim of this study is to compare the efficacy of a new apexification method using Mineral Trioxide Aggregate (MTA®) with the reference treatment based on calcium hydroxide repeated stimulations.

NCT ID: NCT00223327 Completed - Clinical trials for Periapical Periodontitis

Measurement of Bite Force in Humans

Start date: March 2005
Phase: Phase 0
Study type: Observational

This protocol is for a clinical trial to evaluate the reliability of the bite fork as a diagnostic instrument in subjects with pulpal necrosis and apical periodontitis.