Clinical Trials Logo

Signs and Symptoms clinical trials

View clinical trials related to Signs and Symptoms.

Filter by:

NCT ID: NCT03221439 Completed - Pain Clinical Trials

Cognitive Functional Therapy for Chronic Low Back Pain

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

There is evidence, of a single randomized controlled trial, that CFT is better than combined manual therapy and motor control exercise for chronic low back pain. However, this study had significant methodological shortcomings regarding the failure to carry out the intention to treat analysis and a considerable loss of follow-up of patients. It is important to replicate this study through a randomized clinical trial with similar objectives in another domain, but correcting these methodological shortcomings. Therefore, the aim of the study is to assess the efficacy of Cognitive Functional Therapy in patients with chronic non specific low back pain.

NCT ID: NCT03211390 Completed - Clinical trials for Nervous System Diseases

Using Telemedicine to Improve Spasticity Diagnosis Rates

Start date: January 30, 2018
Phase:
Study type: Observational

The purpose of this study is to test the reliability of using telemedicine so a neurologist can remotely identify residents of a long-term care facility who should be referred to a neurologist for an in-person spasticity consultation.

NCT ID: NCT03209960 Completed - Clinical trials for Nervous System Diseases

Validity and Inter-Rater Reliability of a Novel Bedside Referral Tool for Spasticity

Start date: January 30, 2018
Phase:
Study type: Observational

The purpose of this study is to improve spasticity diagnosis through development of a simple physical examination guide for primary care providers to identify patients who would benefit from being referred to a movement disorders neurologist for a spasticity evaluation.

NCT ID: NCT03161392 Completed - Female Clinical Trials

Correlation of Solitary Dilated Duct at Mammography With Ultrasonography and Anatomopathological Findings

Start date: March 16, 2016
Phase:
Study type: Observational

Mammograms performed at the Diagnostic Imaging Department of the "Instituto Brasileiro de Controle do Câncer" (IBCC - Brazilian Cancer Control Institute) will be prospectively evaluated. Patients who present a solitary dilated duct visualized by mammography will be submitted to breast ultrasonography. In case of detection of lesion, a percutaneous biopsy will be performed.

NCT ID: NCT03104894 Completed - Clinical trials for MGD-Meibomian Gland Dysfunction

The Effect of Meibomian Glands Massage on Signs and Symptoms of Dry Eye

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

The study aims to investigate whether combined treatment of MGD massage and artificial tears will improve signs and symptoms of dry eye compared to artificial tears alone. The meibomian glands secrete meibum which is the oily component of the tear film layer. The meibum plays a pivotal role in preventing tear evaporation and smoothening the tears film . Meibomian gland dysfunction is a common condition that affects 39%-50% of the population. It is part of inflammatory disease of the eyelids called blepharitis. Associated syndromes are rosacea and dry eye syndrome . Sign and symptoms are: irritation, hyperemia, burning sensation, photophobia, epiphora and blur. Spectrometry analysis shows change it the fatty acids conformation such as increase in levels of branched-chain fatty acids and decrease in saturated fatty acids . Subsequently the clotted meibum results in glands blockage that can be graded in 0-4 grade scale: grade 2- meibum secretion thick and oily, grade 3- meibum secretion granular-toothpaste like. Although MGD is not often accompanied with inflammatory signs it is a common cause for evaporative dry eye.

NCT ID: NCT03043911 Active, not recruiting - Clinical trials for Signs and Symptoms, Respiratory

Improved Patient Safety Through Continuous Bi-channel RR and SpO2 Monitoring With Masimo Patient SafetyNet

SafetyNet
Start date: February 2016
Phase: N/A
Study type: Observational

The investigator intend to perform an observational study, by adding Respiratory Rate monitoring to an already existing Patient SafetyNet system with SpO2 (Oxygen Saturation) and PR (Pulse Rate) monitoring. RRa will be blinded to the clinicians and all RRa alarms will be deactivated. Retrospective analysis of the observational data collected will be utilized to evaluate the potential benefits of additional continuous respiratory rate monitoring.

NCT ID: NCT03009188 Completed - Clinical trials for Genetic Findings in a Chinese Family With ARS

Genetic Findings in a Chinese Family With Axenfeld-Rieger Syndrom

Start date: July 2016
Phase: N/A
Study type: Observational

Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant disorder, characterized by anterior segment abnormalities and systemic abnormalities. To date,two major genes, forkhead box C1 (FOXC1) on chromosome 6p25 and pituitary homeobox 2 (PITX2) on chromosome 4q25, have been demonstrated to cause ARS. In this study, we performed complete ophthalmologic examinations and analysis of FOXC1 and PITX2 of a Chinese family with ARS.

NCT ID: NCT03003403 Completed - Obesity Clinical Trials

Balance: A Pragmatic Trial of a Digital Health Intervention to Prevent Weight Gain in Primary Care

Start date: January 2017
Phase: N/A
Study type: Interventional

Up to 50% of obese patients are not interested in, or ready for, weight loss. Clinical practice guidelines clearly recommend that these patients avoid gaining weight. However, despite this clinical guideline, weight gain prevention interventions are not available in primary care practice. Balance is a pragmatic, randomized controlled effectiveness trial for weight gain prevention for patients within rural community health centers, using a digital health platform.

NCT ID: NCT02928484 Recruiting - Dyspepsia Clinical Trials

Evaluation of the Effect of a Probiotic Supplement Upon Gastrointestinal Function

Start date: June 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this pilot study is to evaluate whether a probiotic supplement improves gastrointestinal (GI) function.

NCT ID: NCT02913365 Recruiting - Lung Cancer Clinical Trials

Etiologies, Investigations and Outcomes of Patients Presenting With Hemoptysis

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

The study consist of a retrospective analysis of the etiologies, investigations and outcomes of patients presenting between 2005 to 2010 with hemoptysis in a North-American Tertiary center.