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NCT ID: NCT01746355 Completed - Clinical trials for Atypical Facial Pain or Atypical Odontalgia

Assessment and Treatment Patients With Atypical Facial Pain Trough Repetitive Transcranial Magnetic Stimulation

EMTr-AFP
Start date: March 2011
Phase: N/A
Study type: Interventional

Atypical Facial Pain is a chronic condition and presents controversies during diagnostic and treatment, between specialist not have consensus about the pathophysiology. It is possible consider this entitie a potential neuropathic cause without pathological signs. It knows the repetitive transcranial magnetic presents good results in the treatment of chronic pain coditions. The aim this study is evaluated the thresholds and excitability cortical in patients with AFP and verify the patterns of improvement in pain for patients undergoing rTMS compared to controls, as well as the therapeutic response to neuromodulation procedures. This enroll 20 patients with DAF and 20 controls treated with rTMS (5 sessions) and evaluated through questionnaires (EDOF clinical record, McGill Pain Questionnaire, Visual Analogue Scale, Inventory of symptoms of neuropathic pain, neuropathic pain DN4 questionnaire, SF -36, brief pain inventory). At the end of the data will be statistically analyzed and expressed as mean and standard deviation, and analyzed by Student's t test, analysis of variance (ANOVA), Tukey-Kramer and Pearson correlation. The level of significance is 5%. The results will be published in journals indexed in the area both nationally and internationally and presented at conferences and scientific meetings.

NCT ID: NCT01745042 Completed - Clinical trials for Postmenopausal Disorder

Anthropometric, Metabolic, Cardiovascular and Symptomatic Profile in Postmenopausal Women

Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to investigate anthropometric, metabolic, cardiovascular and symptomatic profiles in postmenopausal women.

NCT ID: NCT01744782 Completed - Cystinosis Clinical Trials

Safety/Effectiveness Study of Cysteamine Bitartrate Delayed-release Capsules (RP103) in Cysteamine Treatment Naive Patients With Cystinosis

Start date: December 20, 2012
Phase: Phase 3
Study type: Interventional

This was a long-term, open-label study of the safety, tolerability and effectiveness of RP103 in cystinosis patients who were naïve to any form of cysteamine treatment. Participants received RP103 treatment for at least 12 months. U.S. participants transitioned to the commercially approved drug PROCYSBI®. In Brazil, after at least 12 months of study participation and upon approval by the Brazilian regulatory authorities, participants were eligible to transition to a post-study drug supply program, and continue to receive the drug at no personal cost.

NCT ID: NCT01744756 Completed - Recurrent Pterygium Clinical Trials

Subconjunctival Bevacizumab and Recurrent Pterygium

BRP
Start date: February 2012
Phase: Phase 2/Phase 3
Study type: Interventional

A study to research whether subconjunctival bevacizumab injection may potentially suppress neovascularization in pterygium, retarding and decreasing the size of recurrent pterygium.

NCT ID: NCT01743911 Completed - Hypertension Clinical Trials

Tadalafil Effects in Left Ventricle Diastolic Dysfunction in Resistant Hypertensive Patients

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

Left ventricle diastolic dysfunction (LVDD) is associated with resistant hypertension. In addition, brain natriuretic peptide (BNP) levels are elevated when LVDD is present. It has been shown that phosphodiesterase-5 (PDE5) inhibition improves left ventricle diastolic function in hypertensive rats, despite any difference in blood pressure levels. Also, left ventricle diastolic function enhancement reduces BNP concentration in hypertensive patients. However, it is unknown if these effects exists in humans with resistant hypertension. Therefore, this study was developed to evaluate if the use of a PDE5 inhibitor (tadalafil) for 2 weeks improves LVDD and its effects in BNP levels in resistant hypertensive patients.

NCT ID: NCT01743443 Completed - Keratoconus Clinical Trials

Corneal Sensitivity Cross-linking Keratoconus

CSK
Start date: March 2009
Phase: Phase 2/Phase 3
Study type: Interventional

To evaluate corneal sensitivity changes following corneal cross-linking (CXL) in patients with progressive lower stage keratoconus.

NCT ID: NCT01743183 Completed - Hypertension Clinical Trials

Influence of Respiratory Muscle Training in Elderly Hypertensive Women With Respiratory Muscle Weakness

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

This study aims to evaluate pulmonary function and respiratory muscle strength in a group of elderly women with hypertension before and after a respiratory muscle training.

NCT ID: NCT01742559 Completed - Pain Clinical Trials

The Anesthetic Effect of Anterior Middle Superior Alveolar Technique

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

Anesthesia of the soft and hard tissues in the maxilla may require up to five injections. Thus, the aim of the present study was to evaluate the anesthetic efficacy in buccal tissues after the use of the anterior middle superior alveolar (AMSA) and supraperiosteal techniques during subgingival scaling and root planning (SRP).

NCT ID: NCT01741987 Completed - Dry Eye Clinical Trials

Osmoprotective Containing Lubricants in Dysfunctional Tear Syndrome and Post Refractive Surgery Patients

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

The purpose of this project is to determine the effectiveness of an eyewash osmoprotective lubricant comparing to castor oil containing and non-osmoprotective lubricants in different types of DTS and post refractive surgery patients.

NCT ID: NCT01741402 Completed - Elderly Clinical Trials

Effects of Training in a Virtual Environment in Healthy Elderly

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

The objective of this work was to compare the effects of two balance training programs, one Nintendo Wii Fit-based and the other traditionally-based without the use of a gaming system, on the (1) balance, (2) gait, (3) functionality and (4) cognition ability in older adults. It is a prospective, single blinded, randomized clinical trial performed at Center of Research of the courses of Speech Therapy, Physical Therapy and Occupational Therapy of São Paulo University. Thirty-two older adults are randomly in control and experimental group, 16 each one. The study includes only participants scoring at least 24 in the Mini-Mental State Examination to rule out effects of dementia; without the presence of depression, according to the Geriatric Depression Scale of Yesaváge - version 15 (GDS-15 ≤ 5) and scores on the Berg Balance Scale (EBB ≥ 41).