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NCT ID: NCT03547973 Recruiting - Clinical trials for Metastatic Urothelial Cancer

Study of Sacituzumab Govitecan in Participants With Urothelial Cancer That Cannot Be Removed or Has Spread

TROPHY U-01
Start date: August 13, 2018
Phase: Phase 2
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of sacituzumab govitecan-hziy monotherapy and with novel combinations in participants with metastatic urothelial cancer (mUC).

NCT ID: NCT03547947 Recruiting - Avascular Necrosis Clinical Trials

Clinical and Radiological Outcomes of Medacta Shoulder System

Start date: June 13, 2018
Phase:
Study type: Observational

This is a post-marketing surveillance on Medacta Shoulder System

NCT ID: NCT03546049 Recruiting - Clinical trials for Bile Duct Obstruction, Extrahepatic

Ultrasound-guided Percutaneous Biliary Drainage Versus Endoscopic Ultrasound-guided Biliary Drainage

PUMa
Start date: December 1, 2018
Phase: N/A
Study type: Interventional

Prospective multi-site study of ultrasound-guided percutaneous biliary drainage and endoscopic ultrasound-guided biliary drainage with implantation of a self-expanding metal stent in patients with malignant, distal bile duct obstruction (PUMa-study)

NCT ID: NCT03545555 Recruiting - Clinical trials for Effects of Kale Ingredients on Lipid Status Parameter

Investigations on the Effect of Kale on the Lipid Status

HypocholKale
Start date: April 13, 2018
Phase: N/A
Study type: Interventional

This intervention study investigates the effects of various kale preparations (dietary supplements) on lipid status parameters. Within the study period of 8 weeks, three blood withdrawals are planned (week 0, 4 and 8) for the volunteers. Lipid status parameters (total cholesterol, HDL cholesterol, LDL cholesterol, triacylglycerides) will be determined in blood. There is a correlation between contents of LDL cholesterol, total cholesterol and triacylglycerides and the risk for cardiovascular diseases (CVD). In contrast, a high content of HDL cholesterol is correlated with a lower risk for CVD. In addition, the contents of apolipoprotein A1 and apolipoprotein B will be analysed.

NCT ID: NCT03540784 Recruiting - Clinical trials for Inflammatory Bowel Diseases

Effects of WB-EMS and High Protein Diet in IBD Patients

Start date: October 1, 2013
Phase: N/A
Study type: Interventional

Patients with inflammatory bowel disease (IBD) often suffer from muscle weakness and a low bone mineral density as a consequence of systemic Inflammation and disease treatment limiting Quality of life in a considerable way. Exercise interventions to build up muscle mass and increasing physical function are promising Tools to improve the whole muscular Status of those patients. However, in the acute Phase of IBDs conventional Training methods may be too strenous, also because patients are suffering from acute gastrointestinal symptoms and feel fatigued. Due to those symptoms, patients present low Food intake and great loss of nutrients and energy especially by diarrhea. Individualized nutritional Support may be helpful to avoid malnutrition. The aim of this pilot study is to investigate the effect of a combined exercise and Nutrition Intervention using the gentle Training method of whole-body electromyostimulation (WB-EMS) combined with a individual high Protein nutritional Support on muscle mass, Body composition, physical function, Quality of life and gastrointestinal symptoms in outpatients with IBD.

NCT ID: NCT03539133 Recruiting - Clinical trials for ST-segment Elevation Myocardial Infarction (STEMI)

Systemic Organ Communication in STEMI

SYSTEMI
Start date: October 18, 2017
Phase:
Study type: Observational

Despite progress in pre-hospital care, ambulance logistics, pharmacotherapy and PPCI techniques, ST-segment elevation myocardial infarction (STEMI) continues to confer a substantial burden of morbidity and mortality. Within the STEMI population, there is a spectrum of higher and lower risk patients. The aim of this cohort study is to collect prospectively and systematically clinical research data from STEMI patients. This cohort study is an open-end observational study to identify master switches in myocardial ischemia.

NCT ID: NCT03536234 Recruiting - HIV-1-infection Clinical Trials

Efficacy and Safety of GnRH Analogue Triptorelin for HIV-1 Reservoir Reduction in ART Treated HIV-1 Infected Patients

Start date: September 19, 2018
Phase: Phase 2
Study type: Interventional

An open, randomised, parallel arm phase IIa study. 52 HIV-1 infected patients will be randomised (in a 1:1 ratio) to either an active group or a control group. The active group will receive the GnRH analogue triptorelin depot monthly at baseline, week 4 and week 8. Patients in the active group and in the control group will continue their triple combination antiretroviral therapy (ART) during the study without changes; unless there is rationale for change on medical ground. In order to prevent the negative effects of a low testosterone level, patients in the active group will be offered to receive a single intramuscular depot injection of testosterone approximately 7 days after triptorelin treatment. This depot administration will keep the serum testosterone on a normal level until the next triptorelin dose. This will be repeated when triptorelin is administered at week 4 and week 8. Total study period is 24 weeks.

NCT ID: NCT03534570 Recruiting - Heart Diseases Clinical Trials

Gated Radiotherapy in Left Sided Breast Cancer Patients

GATTUM
Start date: May 2018
Phase:
Study type: Observational

To assess the need of respiratory gated radiotherapy in left sided breast cancer patients.

NCT ID: NCT03532633 Recruiting - Prematurity Clinical Trials

Supply With Micronutrients (Purine and Pyrimidine) in Infants: a Prospective and Observational Study

Start date: March 1, 2017
Phase:
Study type: Observational

Concentrations of micronutrients (especially purine and pyrimidine) in cord blood, blood of mothers and infants and human milk is studied

NCT ID: NCT03528889 Recruiting - Cerebral Palsy Clinical Trials

Controlling Femoral Extension and Derotation Osteotomy In Cerebral Palsy With Electromagnetic Tracking

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

The study is designed to evaluate the use of electromagnetic tracking in multi plane femoral osteotomies, namely extension derotation osteotomies. The goal is to raise the precision of the surgical procedure in order to improve the outcome in short- and long term. All patients are examined with an instrumented 3D gait analysis pre- and one year postoperatively. The electromagnetic tracking system is evaluated against a base line CT or MRI scan serving as reference standard pre- and postoperatively.