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NCT ID: NCT03012711 Not yet recruiting - Clinical trials for Anterior Cruciate Ligament Injury

The Effects of Neuromuscular Exercise Training on Core Stability and Hip Strength in Healthy Adolescent Females

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

This study is an evaluation of the effects of a Neuromuscular training program on hip strength and core stability. It is a randomized clinical trial evaluating pre and post scores.

NCT ID: NCT03010709 Not yet recruiting - Clinical trials for Subarachnoid Hemorrhage, Aneurysmal

Multimodality Monitoring Directed Management of Aneurysmal Subarachnoid Haemorrhage

MMMSAH
Start date: February 2017
Phase: N/A
Study type: Observational

Aneurysmal subarachnoid haemorrhage (aSAH) affects up to 10,000 individuals per year in the UK. It accounts for ~5% of strokes, but is responsible for about 25% quality-adjusted life years (QALYs) lost due to stroke. Although early repair of ruptured aneurysms and aggressive postoperative management has improved overall outcomes, it remains a devastating disease with mortality approaching 50%. Survivors are left with neurological injuries that range from subtle cognitive deficit to disabling cerebral infarctions, less than 60% them returning to functional independence. SAH triggers a series of pathological processes resulting in neuronal damage and consequent neurological deficit termed early brain injury (EBI). Many of the patients who survive the initial bleed, deteriorate days later from delayed ischaemic neurological deficit (DIND), which causes poor outcome or death in up to 30% of patients with SAH. Both of these pathological processes are still poorly understood which limits the number of treatment options. DIND is treated with blood pressure augmentation to ensure adequate blood flow in the brain. In awake patients, response can be easily and accurately assessed by performing a thorough neurological examination. In patients whose clinical condition demands sedation, intubation and ventilation, assessing response to treatment using the neurological examination is virtually impossible. Multimodality monitoring (MM), primarily microdialysis and brain tissue oxygen tension with catheters inserted into the relevant parts of the brain offer direct assessment of both delivery and utilisation of metabolic substrates at the cellular level. These can be used for early detection of DIND as well as monitoring during blood pressure augmentation. The aim of this study is to establish and validate a clinical protocol for MM derived management of SAH patients, to determine optimal therapies for correcting abnormalities in brain metabolism and explore the relationship between MD and other monitoring modalities.

NCT ID: NCT03008798 Not yet recruiting - Clinical trials for Occlusion and Stenosis of Unspecified Cerebral Artery

Prevention for the Restenosis of Intracranial Artery Stent Implantation Treated With Herbal Medicine C117

PRISIT
Start date: January 2017
Phase: Phase 2
Study type: Interventional

Prevention for the Restenosis of Intracranial artery Stent Implantation Treated with herbal medicine C117--PRISIT Trial

NCT ID: NCT03008720 Not yet recruiting - Hemiparesis Clinical Trials

Evaluation of Electrical Activity Tibial Muscle and Postural Control of Individuals With Hemiparesia Post TDCS Associated With FES

Start date: February 2017
Phase: Phase 2
Study type: Interventional

Introduction: It is suggested that increased cortical activity, induced by cerebral stimulation associated or not with other rehabilitation techniques, may potentiate the motor and functional therapeutic effects in individuals with neurological deficits. Objectives: To evaluate the electrical activity of the anterior tibial muscle (TA) and postural control of individuals with hemiparesis due to stroke following treatment with transcranial direct current (tDCS) stimulation and functional electrical stimulation (FES), associated or isolated). (EMG) and postural control by the Balance Evaluation Systems Test (BESTest). Both of which were collected at four different time points: pre-treatment, immediately after 10 treatment sessions, and 30 days follow-up after the interventions. Patients will be randomized into 4 experimental groups: tDCS anodic active + active FES+ active contraction TA, tDCS sham + active FES+ active contraction TA, tDCS anodic active+ placebo FES+ active contraction TA, tDCS sham+ FES sham+ active contraction TA. tDCS (2mA) will be applied over the motor (Cz) and cathodic vertex over the supraorbital region of the normal hemisphere and FES over hemiparetic TA by a researcher who will not be the one who will evaluate the anesthesia patient. The treatment will last 10 sessions, twice a week, with a time of 20 minutes.

NCT ID: NCT03007914 Not yet recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effect of Traditional Chinese Medicine on Outcomes in COPD Patients

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

The aim of this study is to compare the effectiveness of the treatments in two cohort for COPD patients: one, traditional Chinese medicine (TCM) cohort, which have been evaluated and have certain effect; the other, conventional medicine treatments cohort, based on 2015 Global Initiative for Chronic Obstructive Lung Disease (GOLD).

NCT ID: NCT03007706 Not yet recruiting - Clinical trials for Postpartum Infectious Morbidity in Cesarean Section Delivery

Role of Skin Cleansing and Prophylactic Antibiotic in Preventing Infectious Morbidity After Cesarean Section Delivery

Start date: January 2017
Phase: N/A
Study type: Observational [Patient Registry]

This study aims to determine the effectiveness of skin cleansing and prophylactic antibiotics given to women undergoing a cesarean section for reducing the incidence of postpartum infectious morbidity and to assess potential maternal adverse effects and any impact on the infant.

NCT ID: NCT03007342 Not yet recruiting - Clinical trials for Symptomatic Periapical Periodontitis

Effect of Amoxicillin/Clavulanic Acid Combination on Postoperative Endodontic Pain

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

The aim of this prospective, randomized, placebo controlled study is to evaluate the effect of amoxicillin/clavulanic acid combination on post-operative pain and swelling in adult patient with symptomatic apical periodontitis.

NCT ID: NCT03005236 Not yet recruiting - Clinical trials for Kidney Transplant Failure and Rejection

AGe-adapted Benefits of Envarsus Versus Twice-daily Tacrolimus ImmunosuppressioN druGs After Kidney Transplantation

AGEING
Start date: April 2017
Phase: Phase 4
Study type: Interventional

The proportion of elderly patients with end-stage kidney disease undergoing renal replacement therapy (RRT) is steadily increasing. Although kidney transplantation remains the optimal RRT of choice, it is clear that older adults have a differential risk versus benefit profile after kidney transplantation compared to younger adults. No age-adapted immunosuppression for older adults has been shown to improve kidney allograft outcomes but recent sub-analyses of clinical trial data has hinted at improved outcomes for older kidney transplant patients receiving Envarsus versus standard twice-daily tacrolimus formulations. This feasibility study will investigate this effect to see whether a full scale randomised controlled trial is warranted and to provide information regarding study feasibility.

NCT ID: NCT03001960 Not yet recruiting - Clinical trials for Aortic Valve Stenosis

Dual AntiPlatelet Therapies for Prevention of Periinterventional Embolic Events in TAVI

DAPT-TAVI
Start date: March 2017
Phase: Phase 3
Study type: Interventional

TAVI is increasingly adopted as standard treatment for many subgroups of patients with aortic stenosis. However, due to a lack of data there is yet no TAVI-specific guidance regarding the optimum periinterventional drug regimen. The study evaluates the effect of dual antiplatelet pretreatment on periinterventional embolic cerebral lesions and bleeding complications in patients undergoing transfemoral aortic valve implantation (TF-TAVI).

NCT ID: NCT02999880 Not yet recruiting - Clinical trials for Poor Aesthetics of Existing Restoration

Layering Technique Selection for Ultimate Aesthetics in Anterior Composites

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

the importance of this study is to evaluate the clinical performance of direct anterior resin composite restoration constructed using innovative esthetic dual-shade technique and another restoration constructed using polychromatic natural layering technique with various finishing and polishing steps. The benefit from carrying out this study is to help the practitioners to decide the most suitable, easy, perfect technique to provide an optimally aesthetic, long lasting with superior clinical performance direct anterior resin composite restoration.