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NCT ID: NCT01315535 Recruiting - Clinical trials for Obstructive Sleep Apnea Syndrome

Fast Titration of Oral Appliance at Obstructive Sleep Apnea Syndrome (OSAS) Treatment

Start date: March 2011
Phase: N/A
Study type: Observational

The literature does not discuss if the fast oral appliance titration (30 days period) in Obstructive Sleep Apnea Syndrome (OSAS) treatment, may improve subjects quality of life in such brief period. Temporomandibular dysfunction-related (TMD) is one of the most important side effects observed in OSAS treatment with oral appliance. Since the effectiveness of mandibular exercises in the control of TMD pain has already been verified, it may play a fundamental role in the support of the fast oral appliance titration.

NCT ID: NCT01315197 Completed - Low Back Pain Clinical Trials

Massage for Low Back Pain in Nursing Staff

Massage
Start date: October 2010
Phase: N/A
Study type: Interventional

Objectives: Semi experimental Clinical Trial aimed at verifying the effectiveness of massage for lower back pain occupational as well as to assess the influence of technique in performing work activities and life in the team nursing.

NCT ID: NCT01315041 Completed - Clinical trials for Menopausal Symptom Relief

"Pi" and Hot Flushes

Start date: December 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Hot flushes are common symptoms in women after menopause, and are important causes of discomfort and lead to high number of medical consultations. Hormone replacement therapy is an effective treatment, however it can bring undesirable consequences and may be contraindicated for some women. Options are inhibitors of serotonin or serotonin-norepinephrine reuptake, gabapentin, herbal medicines and homeopathy. None of these therapies is widely accepted of effective. Therefore, the search for new therapeutic options is highly desirable. Ingestion of malagueta pepper fruits (Capsicum frutescens L. var. malagueta) causes sensations similar to those experienced by menopausal women during hot flushes. By the principle of homeopathy, "the like cures the like", the objectives of this study are: (a) to determinate whether pathogenesis of a homeopathic medicine made from C. frutescens fruits include symptoms like hot flushes, and (b) whether this medicine is effective on hot flushes relief in women after menopause. There will be 2 distinct phases. Phase 1 is the determination of the medicine's pathogenesis in healthy volunteers, in a randomized placebo-controlled, double-blind design. Phase 2 is the investigation of the medicine's effects on hot flushes of women after menopause, in a randomized placebo-controlled, double-blind design. The investigators expect a significant reduction on symptoms perception, assessed by internationally validated tools. The study is expected to last for 18 months, with 36 patients included in each phase.

NCT ID: NCT01314924 Completed - Hypertension Clinical Trials

Effects of Acute Ingestion of Dark Chocolate on Endothelial Function in Hypertensive Patients

Start date: January 2011
Phase: Phase 4
Study type: Interventional

We aimed to identify clinical and vascular parameters of treated hypertensive patients who present beneficial effects of dark chocolate for one-week period on vascular function.

NCT ID: NCT01314196 Completed - Clinical trials for Shoulder Impingement Syndrome

Progressive Resistance Training of the Biceps in Subacromial Impingement Syndrome

PRTB
Start date: December 2008
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate the influence of progressive resistance training of the biceps in shoulder rehabilitation in patients with subacromial impingement syndrome (SIS). Method: a randomized controlled clinical trial, with analysis intention-to-treat, approved by the Ethics and Research (1019/08), containing sixty patients of both sexes, SIS, evaluated at the initial time (T0), with 45 days (T45) and 90 days of treatment (T90). We analyzed the pain at rest (VAS), range of shoulder movement, strength, function by The Disabilities of Arm, Shoulder and Hand (DASH) and quality of life by Short Form-36 (SF-36) and Western Ontario Rotator Cuff Index (WORC). They recommended the use of NSAIDs and analgesics in the presence of pain exacerbated, every eight hours. Study groups will perform therapeutic exercises for the shoulder and scapula stabilizers. In the experimental group associate progressive resistance training of the biceps.

NCT ID: NCT01314170 Not yet recruiting - Glaucoma Clinical Trials

Evaluation of Efficacy and Safety of Susanna Implant in Patients With Refractory Glaucoma.

Start date: May 2011
Phase: Phase 3
Study type: Interventional

Study clinical multicenter, phase III, open-label, prospective character to evaluate the efficacy and safety Susanna Implant in patients with refractory glaucoma.

NCT ID: NCT01314157 Completed - Clinical trials for Chronic Low Back Pain

Evaluation of Isostretching Effects in Patients With Mechanical and Postural Chronic Low Back Pain

Start date: March 1, 2011
Phase: N/A
Study type: Interventional

Isostretching is effective in treating chronic back pain to improve pain, quality of life and functional capacity.

NCT ID: NCT01313702 Withdrawn - Clinical trials for Cardiovascular Disease

Single Pill to Avert Cardiovascular Events

SPACE
Start date: October 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether a polipill improved the compliance with treatment compared to usual care that use two or more drugs,in patients at high cardiovascular risk or previous cardiovascular disease.

NCT ID: NCT01313572 Terminated - Clinical trials for Coronary Artery Disease

Study of the Safety and Efficacy of Apadenoson for Detection of Myocardial Perfusion Defects Using SPECT MPI

ASPECT2
Start date: August 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see whether apadenoson is as effective as adenosine when used as a pharmacological stress agent in myocardial SPECT-imaging (SPECT-MPI)to detect defects in the supply of blood to the heart muscle (myocardial perfusion defects). The study will also look at whether apadenoson is better tolerated than adenosine when used in SPECT-MPI.

NCT ID: NCT01312194 Completed - Clinical trials for Periapical Periodontitis

Periapical Healing After One or Two-visits to Endodontic Treatment in Adolescents Patients

PHAP
Start date: May 2004
Phase: N/A
Study type: Interventional

The main objective of this study is the prevention and repair of apical periodontitis in lower molars with pulp necrosis after the execution of endodontic treatment in one or two visits in adolescent patients. Moreover, it is also observed the frequency of postoperative pain in endodontic treatment.