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Tooth Diseases clinical trials

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NCT ID: NCT02561702 Completed - Clinical trials for Charcot Marie Tooth Disease

Mexiletine for Muscle Cramps in Charcot Marie Tooth Disease

Start date: September 2015
Phase: Phase 2
Study type: Interventional

Charcot Marie Tooth Disease is a family of inherited peripheral neuropathies, with over 70 causative genes identified to date.1-4 Muscle cramps are frequent in CMT, affecting up to 85% of patients with some subtypes of CMT. These cramps impact quality of life and have been identified as an important therapeutic target for clinical trials in CMT.1-4 There is no FDA approved treatment for muscle cramps.5 Mexiletine is a sodium channel blocker approved for treatment of arrhythmias. As a sodium channel blocker, mexiletine offers the promise of effective therapy for muscle cramps.

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: 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).

NCT ID: NCT01925339 Completed - Dental Implant Clinical Trials

Esthetic Outcomes of Immediately Placed Implants Receiving Immediate Provisionalization and Delayed Restoration

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

The purpose of this study is to compare two different timings of restoring dental implants that are placed right after tooth extraction: The test group will have the provisional crown placed at the time of implant placement. The control group will have the tooth removed and the implant placed at the same appointment but restorations placed after 4 months. Both procedures currently are accepted methods for replacing missing teeth but direct comparisons of the two procedures are lacking. The results of this study should aid clinicians in selecting the best timing for restoring implants for their patients. The hypothesis is that immediate restoration might increase aesthetic outcomes, e.g. less mucosal recession.

NCT ID: NCT01827098 Completed - Clinical trials for Dental Pulp Necrosis

A Clinical Study to Compare Two Revascularization Protocols to Treat Non-vital Teeth With Incomplete Root Formation

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

Both methods tested in this study disinfect the non-vital root canals and induce blood clot formation inside the root canal. One method places calcium hydroxide inside the root canal after disinfection and the blood clot is induced four weeks later. The other method performs disinfection and induction of blood clot in one appointment. The investigators hypothesize that both methods will obtain the same success rate in eliminating infection, increase in root length and canal walls thickness.