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Bell Palsy clinical trials

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NCT ID: NCT01686464 Completed - Bell's Palsy Clinical Trials

A Clinical Study on the Combined Magnetic and Oxygen Treatment for Bell's Palsy

Start date: June 1998
Phase: N/A
Study type: Interventional

The aim of this clinic trial is to testify the efficacy of using new and noninvasive therapy, called simultaneous "Magnetic and Oxygen Treatment along Meridians and Collaterals" (MOMC), to treat Bell's Palsy.

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: 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: NCT00989209 Completed - Facial Paralysis Clinical Trials

Myofunctional Therapy in Facial Palsy

Start date: January 2005
Phase: N/A
Study type: Interventional

Objective: Quantify the benefits of myofunctional therapy associated to botulinum toxin injection in patients with long standing facial unilateral palsy.

NCT ID: NCT00903669 Completed - Clinical trials for Peripheral Facial Paralysis

Anthropometric Angular Measurement to Determine Muscle Tonus in Patients With Peripheral Facial Paralysis

PF
Start date: January 2005
Phase: N/A
Study type: Observational

The current study sought to determine the reliability of the rehabilitation protocol using the labial commissure angle (LCA) as an indicator of both muscle tonus and therapeutic success. The investigators hypothesized that this measurement would provide objective data regarding the efficacy of rehabilitation for these challenging patients.

NCT ID: NCT00685789 Completed - Bell's Palsy Clinical Trials

Acupuncture With Deqi And Psychological Effects in Treatment of Bell's Palsy

ADAPT
Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to observe the influence of Deqi and neuropsychological factors on effects of acupuncture treatment for Bell's Palsy.

NCT ID: NCT00608660 Completed - Bell's Palsy Clinical Trials

Randomized Controlled Trial of Acupuncture to Treat Bell's Palsy According to Different Stages

Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of this trial will certify the efficacy of using staging acupuncture and moxibustion to treat Bell's Palsy

NCT ID: NCT00561106 Completed - Bell´s Palsy Clinical Trials

Prednisone-Placebo vs Prednisone-Valacyclovir in Bell´s Palsy

PVBP
Start date: December 2002
Phase: N/A
Study type: Interventional

Since steroids carry a moderate beneficial effect in Bell's palsy, and to address this question, valacyclovir was added to prednisone for the treatment of this condition.

NCT ID: NCT00510263 Completed - Bell's Palsy Clinical Trials

Scandinavian Bell's Palsy Study

SBPS
Start date: May 2001
Phase: Phase 4
Study type: Interventional

The main objective of this study is to study the effects of prednisolone and valaciclovir, with equal importance, compared to placebo for the treatment of Bell´s palsy. The combination of prednisolone and valaciclovir will also be studied.

NCT ID: NCT00438087 Completed - Facial Palsy Clinical Trials

Corticosteroids in Prevention of Facial Palsy After Cranial Base Surgery

Start date: March 2007
Phase: Phase 3
Study type: Interventional

Facial palsy after surgical removal of cranial base tumors adherent to the nerve can partly be explained by inflammation.