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Facies clinical trials

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NCT ID: NCT01591304 Completed - Facial Acne Clinical Trials

Feasibility Study: Ulthera® System for the Treatment of Moderate to Severe Facial Acne

Start date: August 2011
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of Ultherapy for the treatment of facial acne.

NCT ID: NCT01566396 Completed - Facial Wrinkles Clinical Trials

Evaluation of Safety and Efficacy of the 3F Applicator (A3F) for Treatment of Facial Wrinkles

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

The 3F Applicator (A3F) is indicated for use in dermatological procedures requiring ablation and resurfacing of the skin, and for the treatment of facial wrinkles. This study was designed in order to evaluate the safety and efficacy of the A3F for treatment of facial wrinkles.

NCT ID: NCT01547273 Completed - Clinical trials for Facial Gingival Profile

The Effect of Bone Grafts on Facial Gingival Profile in Maxillary Anterior Single Tooth Replacement

Start date: March 20, 2012
Phase: N/A
Study type: Interventional

The purpose of this investigator-initiated study is to evaluate the facial gingival profile following immediate implant placement and provisionalization in conjunction with connective tissue graft with or without bone graft

NCT ID: NCT01537952 Completed - Facial Paralysis Clinical Trials

Microbiologic Findings of Acute Facial Palsy in Children

Start date: May 2007
Phase: N/A
Study type: Observational

Objective: Microbiologic etiologies of facial palsy in children were investigated. Study design: Prospective clinical study. Methods: Forty-six children aged 0-16 years with facial palsy comprised the study group. Paired serum samples and cerebrospinal fluid were tested to find indications (antibodies, growth of the microbe, or nucleic acids) of microbes putatively associated with facial palsy. The microbes tested were herpes simplex virus-1 and -2, varicella-zoster virus, human herpesvirus-6, Mycoplasma pneumoniae, Borrelia burgdorferi, influenza A and B-, picorna-, cytomegalo-, parainfluenza-, respiratory syncytial-, coxsackie B5-, adeno-, and enteroviruses, Chlamydia psittaci, and Toxoplasma gondii. Besides the routine tests in clinical practice, serum and cerebrospinal fluid samples were tested with a highly sensitive microarray assay for DNA of herpes simplex virus-1 and -2, human herpesvirus-6A , -6B, -7, Epstein-Barr-, cytomegalo-, and varicella-zoster viruses.

NCT ID: NCT01345591 Completed - Adipose Tissue Clinical Trials

A Study to Evaluate the Results of Facial Soft Tissue Reconstruction in Patients Who Have Suffered Traumatic Injury

BTI
Start date: September 2009
Phase: N/A
Study type: Interventional

Injuries resulting in facial trauma are common, and can have devastating consequences on your quality of life. While the facial bones can often be reconstructed, physicians strive to find better ways to accurately restore injured facial features. In this clinical trial funded by the Department of Defense, the investigators are evaluating how effectively fat grafting can restore facial features, and how the filling effect of the fat graft lasts over time in participants with visible facial injuries. All procedures for this research study will be performed at the University of Pittsburgh Medical Center.

NCT ID: NCT01327157 Completed - Orofacial Pain Clinical Trials

Study of a New Technique to Improve the Symptoms of Orofacial Discomfort in Patients With Peripheral Facial Paralysis

Start date: March 2009
Phase: N/A
Study type: Interventional

- The purpose of this study was to evaluate the effects of Neuro Occlusal Rehabilitation (RNO) in patients with peripheral facial palsy (PFP) disease, noting the decrease in symptoms of masticatory dysfunction. - According to Carvalho (2009) patients with PFP have chronic unilateral masticatory preference. Santos et al. (2009) in the same year noted that these conditions can lead to problems with temporomandibular disorder. - Hypothesis- known that performing occlusal adjustment in these patients with chronic PFP, ensuring a maximum of dental contacts and a final stop of the masticatory cycle stable, providing a balanced occlusion. - dental cleaning was performed in two groups for the blind study - visual analog scale -To assess the quality of the oral functions of these patients, the investigators applied the visual analog scale(VAS) and statistically evaluated the degree of satisfaction regarding the functions of oro facial in relation to mastication and temporomandibular dysfunction. - gnathostatic models were made in the treatment group in the first and last query. - occlusal adjustment in treatment group.In the group treated occlusal adjustment was made in the teeth and applied a new (VAS) before and after treatment. The RNO, is defined as a part of medicine that operates in stomatology occlusal plane as a guide to a harmonious development of the face, chewing facilitating bilateral and alternating. (Planas, 1997). It works through selective grinding on the occlusal platform, providing an increased number of dental contacts.

NCT ID: NCT01299103 Completed - Facial Rhytides Clinical Trials

Safety and Efficacy of Single Therapy Versus Double and Triple Therapy of the Pellevé™ Wrinkle Treatment System for the Treatment of Moderate Facial Wrinkles

Start date: April 2010
Phase: N/A
Study type: Interventional

This study compares the safety and efficacy of single therapy versus double therapy using the Pellevé™ Wrinkle Treatment System for the treatment of mild to moderate facial wrinkles in Fitzpatrick Skin Types I - IV. Safety is assessed by analysis of adverse events. Efficacy is assessed by change in Fitzpatrick score for facial wrinkles.

NCT ID: NCT01286363 Completed - Facies Clinical Trials

Facial Patterns and Masticatory Symmetries

Start date: September 2006
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate chewing side preference, and lateral asymmetry of occlusal contact area and bite force of individuals with different craniofacial patterns

NCT ID: NCT01281267 Completed - Clinical trials for Severe Facial Deformity

Face Transplantation for Treatment of Severe Facial Deformity

Start date: September 1, 2009
Phase: N/A
Study type: Interventional

Face transplantation surgery is the transfer of face tissue from a deceased human donor to a patient with a severe facial deformity. Face transplantation is an innovative reconstructive procedure that has the potential to significantly improve the lives of patients with severe facial injuries. The purpose of this study is to develop the best practices for facial transplantation that will improve the outcomes of future face transplant recipients.

NCT ID: NCT01269164 Completed - Clinical trials for Severe Facial Deformities

Face Transplantation Clinical Trial

Start date: July 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to apply human facial allograft transplant to the subjects with severe facial deformities or disfigurements in order to provide adequate coverage, aesthetic appearance and functional outcome.