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NCT ID: NCT02505672 Not yet recruiting - Clinical trials for Nasopharyngeal Carcinoma

Vestibular Function After Chemoradiotherapy for Nasopharyngeal Carcinoma

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

Nasopharyngeal carcinoma (NPC) is usually treated with chemoradiotherapy. While the effects of this treatment on cochlear function is well characterized, its effect on vestibular function is not well studied. In this study the investigators will study the vestibular function of 50 patients undergoing chemoradiotherapy for NPC both before and after treatment in order to better define its effects. All patients will undergo a validated questionnaire (dizziness handicap index), posturography, audiometry and vestibular-evoked myogenic potentials.

NCT ID: NCT02499419 Not yet recruiting - Clinical trials for Mitral Valve Prolapse

Exercise Capacity Evaluation in Patients With Non-rheumatic Mitral Valve Prolapse (MVP)

Start date: September 2015
Phase: N/A
Study type: Observational

Mitral valve prolapse (MVP) is a relatively common cardial problem in which one or more of the leaflets of the mitral valve prolapse during systole into the left atrium. The disease is very heterogeneous and can vary from a benign disease with almost no impact on the patient's life to a severe cardiac problem with many complications and high mortality rate. The purpose of the study is to see if the investigators can find a relation between the severity of the MVP to the exercise capacity of the patient. The investigators also want to see if they can find a difference between the exercise capacity of mild MVP patients and healthy people. To evaluate the exercise capacity of the subjects the investigators use Cardiopulmonary Exercise Testing (CPET). CPET is probably the best known way to get a full picture of the subject's functions during exercise. By combining gas exchange monitoring and ECG during a controlled exercise in which the subject reaches maximal effort, the test gives information about the cardiac, the pulmonary and the metabolic functions of the subject. This information can help identify if there is a problem to perform exercise properly and more specifically if the limitation is due to a cardiac, pulmonary or metabolic problem.

NCT ID: NCT02498366 Not yet recruiting - Rhabdomyolysis Clinical Trials

Exertional Rhabdomyolysis- Characterization of Prediction Tests for Return to Duty

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

In order to determine norm values for skeleton muscle disassembly due to physical exertion in healthy and trained population, and developing a prediction test for approval for rhabdomyolysis injuries to return to duty, 50 healthy subjects will undergo a series of different physical tests.

NCT ID: NCT02498223 Not yet recruiting - Work Load Clinical Trials

Adjusting the Load Carried by the Soldier According to Body Composition Measurements and Aerobic Capacity

LCI
Start date: September 2015
Phase: N/A
Study type: Interventional

In order to reduce the physiological and biomechanical loads that the soldiers are exposed to, the investigators want to examine new approaches for distributing the carried loads according to measurements that are specific for each soldier (body composition and aerobic capacity). A functional index (LCI=load carriage index) will provide the commander a tool for better decisions in distributing the same total load among the same number of soldiers, according to each soldier's ability.

NCT ID: NCT02498158 Not yet recruiting - Clinical trials for Functional Neural Connectivity

Functional Neural Connectivity at Rest as a Diagnostic Tool for Intolerance to Heat

fMRI
Start date: September 2015
Phase: N/A
Study type: Observational

Functional neural connectivity at rest of 3 groups (heat tolerant, heat intolerant and healthy subjects) will be assessed using the anatomical and functional MRI scans and compared.

NCT ID: NCT02497820 Not yet recruiting - Clinical trials for Lynch Syndrome I (Site-specific Colonic Cancer)

Finding the Best Dose of Aspirin to Prevent Lynch Syndrome Cancers

CaPP3 Israel
Start date: September 2016
Phase: Phase 3
Study type: Interventional

A randomised double blind dose non-inferiority trial of a daily dose of 600mg versus 300mg versus 100mg of enteric coated aspirin as a cancer preventive in carriers of a germline pathological mismatch repair gene defect, Lynch Syndrome. Project 3 in the Cancer Prevention Programme (CaPP3).

NCT ID: NCT02496845 Not yet recruiting - Clinical trials for Erectile Dysfunction

Safety and Clinical Efficacy of Local Topical Treatment for Erectile Dysfunction

Start date: August 2015
Phase: Phase 1/Phase 2
Study type: Interventional

VL#FIA3-30 is a preparation intended for topical use, applied on the penis, for the treatment of ED.

NCT ID: NCT02494908 Not yet recruiting - Parkinson Disease Clinical Trials

Evidence of Neuroplasticity After Performing a Cognitive Task in Idiopathic Parkinson's Disease Patients

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

As seen in previous studies Diffusion Tensor Imaging (DTI) MRI is able to detect very subtle changes in brain tissue even after a very short timescale of hours resulting from performing a cognitive task and learning, We wish to explore and compare those changes to patients with idiopathic PD (IPD) and see if there are changes in the learning process and can we detect them using widely available noninvasive techniques such as MRI.

NCT ID: NCT02491762 Not yet recruiting - Clinical trials for Breast Reconstruction

The Effect of Breast Reconstruction Surgery Using Tissue Expanders on Respiratory Functions

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

This study evaluates the effect of breast reconstruction surgery on respiratory functions. 45 patients elected for unilateral or bilateral breast reconstruction surgery will go through respiratory function examinations a month prior to the surgery, one month after surgery and three months after surgery.

NCT ID: NCT02477735 Not yet recruiting - Sleep Disturbances Clinical Trials

The Effect of Tympanostomy Tube Insertion on Sleep in Children With Chronic Otitis Media With Effusion

Start date: June 2015
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the prevalence of sleep disturbances in children with Chronic Otitis Media with Effusion (COME) and the effect of tympanostomy tube insertion (TTI) on sleep disturbances.