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Tooth Diseases clinical trials

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NCT ID: NCT02532244 Recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases

Start date: June 2015
Phase:
Study type: Observational

The goal of this study is to establish a genetic registry of patients with early-onset motor neuron and neuromuscular diseases. The investigators will collect samples from patients with a motor neuron or a neuromuscular disorder and their family members. The samples to be collected will be obtained using minimally invasive (whole blood) means. The research team will then extract high quality genomic DNA or RNA from these samples and use it to identify and confirm novel gene mutations and to identify genes which regulate the severity of motor neuron/neuromuscular diseases.

NCT ID: NCT02429947 Completed - Tooth Diseases Clinical Trials

An Analysis of the Symptomatic Domains Most Relevant to Charcot Marie Tooth Neuropathy (CMT) Patients

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

The purpose of this study is to identify the issues that have greatest impact on QOL for patients with Charcot Marie Tooth (CMT) Disease. Patients who have -registered in the Inherited Neuropathies Consortium Contact Registry will be invited to participate.

NCT ID: NCT02293031 Enrolling by invitation - Clinical trials for Alveolar Bone Atrophy

Gene-activated Matrix for Bone Tissue Repair in Maxillofacial Surgery

Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate safety and efficacy of gene-activated matrix ("Nucleostim") for regeneration of bone tissue in maxillofacial area. Patients with congenital and acquired maxillofacial defects (sockets of extracted teeth, bone defects after injuries, surgeries, excision of benign neoplasms and pseudotumors, etc.) or alveolar bone atrophy will be included into the study.

NCT ID: NCT02286648 Recruiting - Pulpitis Clinical Trials

Success Rate Evaluation of Miniature Pulpotomy With MTA in Primary Molars

Start date: February 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the clinical and radiographic success rate of Miniature pulpotomy with Mineral Trioxide Aggregate (MTA) in primary molars.

NCT ID: NCT02194010 Completed - Clinical trials for Charcot Marie Tooth Disease

Disability Severity Scale (DSI) and Hereditary Motor and Sensory Neuropathy Overall Disability Scale (HMSN-R-ODS)

DSI and HMSN
Start date: April 2014
Phase:
Study type: Observational

The purpose of this research study is to create and validate two patient reported outcome (PRO) questionnaires. PRO questionnaires ask questions that help to measure disability in patients with inherited neuropathies. These questionnaires ask questions about what participants think disability is for themselves or others with inherited neuropathies. These questionnaires are a useful tool when evaluating whether treatments are working in the day to day life of an individual, although there are currently no questionnaires available specifically for people who have Charcot Marie Tooth disease (CMT).

NCT ID: NCT02161874 Completed - Partial Edentulism Clinical Trials

Evaluation of Integration Success and Crestal Bone Preservation Biomet 3i's T3 Implant System

OAK
Start date: April 2013
Phase: N/A
Study type: Interventional

This study evaluates the T3 implant system for the preservation of alveolar crestal bone and the establishment of initial integration. The new surface-treated features of the implant may contribute to improved soft and hard tissue healing. The success rate of the T3 implant will be no different than that of the control implant, which possess similar geometry but different surface treatments.

NCT ID: NCT02158377 Completed - Partial Edentulism Clinical Trials

TM vs TSV Implants Loaded Early vs Conventional in Anterior and Posterior Areas

TMEL
Start date: March 2013
Phase: N/A
Study type: Interventional

Randomized-controlled, multicenter study of Trabecular Metal (TM) and Tapered Screw-Vent (TSV) dental implants loaded early in maxillary and mandibular sites.

NCT ID: NCT02011204 Completed - Multiple Sclerosis Clinical Trials

Study of Electrical Impedance Myography (EIM) in ALS

Start date: November 2013
Phase: N/A
Study type: Observational

This trial is studying Electrical Impedance Myography (EIM) for measuring muscle health. The trial is studying people with Amyotrophic Lateral Sclerosis (ALS), other neuromuscular diseases, and healthy volunteers to see if the EIM device can measure disease in muscle tissue.

NCT ID: NCT02001038 Completed - Clinical trials for Charcot-Marie-Tooth Disease

Survey of Current Management of Orthopaedic Complications in CMT Patients

Start date: February 2013
Phase: N/A
Study type: Observational

Charcot-Marie-Tooth (CMT) disease is the most common inherited peripheral neuropathy. Foot deformities are frequent complications in CMT patients and orthopaedic surgery is often required. As yet there are no systematic studies on the management of orthopaedic complications in CMT patients and the current approach varies between centres. This study is a survey with the aim of understanding the current surgical approach to orthopaedic complications in CMT. The target population includes orthopaedic surgeons who perform surgical procedures for foot deformities in CMT patients attending centres participating in the Inherited Neuropathies Consortium (INC).

NCT ID: NCT01929031 Completed - Pain, Postoperative Clinical Trials

Efficacy and Safety of Ibuprofen and Caffeine in Dental Pain

Start date: August 2013
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to compare the efficacy of a combination product containing ibuprofen 400 mg and caffeine 100 mg versus either ingredient alone as well as placebo for the treatment of post-surgical dental pain over an eight-hour period followed by a single dose of study medication (study stage 1). A secondary objective is to evaluate efficacy of multiple doses of the combination in comparison to ibuprofen alone over a 5-day post-surgical period (study stage 2).