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NCT ID: NCT02274701 Not yet recruiting - Clinical trials for Oncology [See Also, Affected System]

Holistic Needs Assessment in Outpatient Cancer Care

Start date: October 2014
Phase: N/A
Study type: Interventional

This study evaluates the impact of holistic needs assessment (HNA) on patient/clinician communication in outpatient cancer care. Half of the participants will complete a HNA prior to their clinical consultation. They will then take it into the consultation and it will inform a discussion around any identified areas of need. Half of the participants will be in the control group meaning there will be no additional intervention they will receive care as normal. The consultations will be audio-recorded. The patient will complete two outcome measures following the consultation.

NCT ID: NCT02270424 Not yet recruiting - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effect of Traditional Chinese Medicine on Outcomes in Patients With Severe / Very Severe COPD

Start date: October 2014
Phase: Phase 3
Study type: Interventional

The aim of this study is to compare the effectiveness of two treatments for severe / very severe COPD patients: one, conventional medicine based on 2013 Global Initiative for Chronic Obstructive Lung Disease (GOLD) and Chinese Treatment Guidelines; the other, TCM treatments and conventional medicine, which have been evaluated and have certain effect.

NCT ID: NCT02269449 Not yet recruiting - Clinical trials for Percutaneous Coronary Intervention

Radial Artery Patency and Bleeding, Efficacy, Adverse evenT Trial

RAPandBEAT
Start date: October 2014
Phase: N/A
Study type: Interventional

The objectives of this study are to demonstrate the safety and efficacy of the new 6Fr sheath (Glidesheath slender; Terumo, Tokyo,Japan ; GSS) compared with the contemporary 5Fr sheath (Hydrophilic coating sheath from Terumo; Tokyo, Japan (standard of care ; SOC).

NCT ID: NCT02264964 Not yet recruiting - Venous Thrombosis Clinical Trials

Duration and Adverse Events of Non-cuffed Catheter in Patients With Hemodialysis

DACAPO
Start date: January 2015
Phase: N/A
Study type: Interventional

The duration and adverse events of non-cuffed catheter in patients with hemodialysis will be investigated by multicenter prospective cohort. Totally, 1,400 patients with chronic renal failure requiring hemodialysis will be enrolled. 900 patients will be given right internal jugular catheterization, and the other 500 patients unsuitable for right internal jugular catheterization will receive femoral catheterizations. Every patient will be followed-up for six months. During following-up period, the duration time and adverse events of non-cuffed catheter will be recorded in details, including inadequate hemodialysis blood flow, venous stenosis, venous thrombosis, infection, catheter thrombosis and so on. The central vein will be evaluated by CT Angiography to identify its stenosis at last visit after 6 months. This multicentre trial will provide evidence to develop guideline for duration time of using non-cuffed catheter.

NCT ID: NCT02263781 Not yet recruiting - Obesity Clinical Trials

PREPL in Health and Disease

PHD
Start date: October 2014
Phase: N/A
Study type: Interventional

Evaluation of PREPL activity in healthy controls and known or possible PREPL deficient patients

NCT ID: NCT02252614 Not yet recruiting - Clinical trials for Postoperative Pain, PCA Contramal Consumption

Efficacy of Intravenous Naproksen Sodium+Codein and Paracetamol+Codein on Postoperative Pain on Postoperative Pain

Start date: September 2014
Phase: Phase 4
Study type: Interventional

Comparition the analgesic effects of intravenous naproksen sodyum+codein with that of paracetamol+codein on postoperative pain and contramal consumption during the first 24 hour after a lumbar disk surgery.

NCT ID: NCT02250846 Not yet recruiting - Clinical trials for Asymptomatic Brain Metastases of Non Small Cell Lung Cancer

Study of EGFR-TKI to Asymptomatic Brain Metastases of NSCLC

EABM
Start date: January 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether EGFR-TKI can control the development of intracranial lesions in Non Small Cell Lung Cancer patients with asymptomatic brain metastases, and the difference in progression free survival between exon 19 and exon 21 mutations.

NCT ID: NCT02247817 Not yet recruiting - Clinical trials for Heart Failure With Intraventricular Conduction Delay

A Combined Transvenous and Epicardial Lead Placement Procedure for Implantation of Cardiac Resynchronization Devices: a Feasibility Study.

Start date: October 2014
Phase: N/A
Study type: Interventional

Cardiac resynchronization therapy has become one of the cornerstones of the treatment of heart failure. However, a large proportion of patients still fails to this type of therapy. This may be due to a suboptimal position of the left ventricular pacing lead, which may be caused by unfavorable cardiac venous anatomy. Implantation of the pacing lead using video assisted thoracic surgery is more flexible and evades the venous system altogether, resulting in a much more favorable position of the pacing lead, with better treatment results as e consequence.

NCT ID: NCT02247713 Not yet recruiting - Clinical trials for Non Small Cell Lung Cancer Stage III

An International Study on the Use of PET/CT in Radiotherapy Planning in Low and Middle Income Countries

PERTAIN
Start date: September 2014
Phase: N/A
Study type: Observational

A part retrospective, part prospective cohort study to assess the difference in 2-year overall survival in patients with stage III NSCLC receiving chemoradiotherapy with curative intent in low and middle income countries before and after a training intervention on the use of PET/CT for radiotherapy treatment planning.

NCT ID: NCT02245334 Not yet recruiting - Infection Clinical Trials

A Prospective Trial of Povidone-iodine Suppository Before Transrectal Ultrasound Guided Prostate Biopsy

Start date: October 2014
Phase: Phase 4
Study type: Interventional

To assess the effect of povidone-iodine on infectious complication rate caused by transrectal prostate biopsy