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NCT ID: NCT02960022 Recruiting - Prostate Cancer Clinical Trials

A Study for Subjects With Prostate Cancer Who Previously Participated in an Enzalutamide Clinical Study

Start date: December 22, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to collect long term safety data in subjects who are continuing to derive clinical benefit from treatment with Enzalutamide from the subjects participation in an enzalutamide clinical study sponsored by Astellas or Medivation (i.e., parent study) which has completed, at a minimum, the primary analysis or the study specified evaluation period.

NCT ID: NCT02932410 Recruiting - Clinical trials for Pulmonary Arterial Hypertension

A Study to Assess Whether Macitentan Delays Disease Progression in Children With Pulmonary Arterial Hypertension (PAH)

TOMORROW
Start date: October 24, 2017
Phase: Phase 3
Study type: Interventional

This is a prospective, multicenter, open-label, randomized, controlled, parallel Phase 3 study with an open-label single-arm extension period to evaluate pharmacokinetics (PK), safety and efficacy of macitentan in children with pulmonary arterial hypertension (PAH).

NCT ID: NCT02901353 Recruiting - Angina Pectoris Clinical Trials

A Prospective, Single-arm, Multi-centre, Observational, Real World Registry

Morpheus
Start date: February 2, 2017
Phase:
Study type: Observational [Patient Registry]

A prospective, single-arm, multi-centre, observational, real world registry to evaluate safety and performance of the BioMime™ Morph Sirolimus Eluting Coronary Stent System for very long coronary lesions.

NCT ID: NCT02894645 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia (ALL)

Malaysia-Singapore Acute Lymphoblastic Leukemia 2010 Study

Start date: October 2008
Phase: Phase 4
Study type: Interventional

The overall objective of this study is to continue to improve the cure rate of childhood acute lymphoblastic leukemia (ALL) in Singapore and Malaysia in the context of a multi-centre cooperative trial using a risk-stratified therapy based primarily on early response to therapy utilizing a simplified minimal residual disease (MRD-lite) platform.

NCT ID: NCT02823821 Recruiting - Clinical trials for End-Stage Kidney Disease

Randomised Evaluation of Sodium Dialysate Levels on Vascular Events

RESOLVE
Start date: June 2016
Phase: Phase 4
Study type: Interventional

This global study will assess the effect of randomising dialysis sites to one of two default dialysate sodium concentrations in current practice, 140mmol/l and 137mmol/l, on major cardiovascular events and death in patients receiving maintenance haemodialysis.

NCT ID: NCT02784405 Recruiting - Clinical trials for Coronary Artery Disease

Self-apposing Stentys Stents Registry

SPARTA
Start date: December 2016
Phase: N/A
Study type: Observational [Patient Registry]

Self-apposing, drug-eluting Stentys coronary stents represent a valuable tool for the treatment of coronary artery stenosis. Their ability to adapt to widely varying vessel calibers and to auto-expand after their release to self-appose to vessel walls is particularly useful in the presence of ectasic coronary arteries or significant vessel tapering. The investigators planned this study to assess the feasibility, the effectiveness and the safety of the implantation of self-apposing, drug-eluting Stentys stents for percutaneous coronary intervention. Consecutive patients undergoing percutaneous coronary intervention with implantation of a self-apposing Stentys stent were enrolled in this multi center registry. Inclusion criteria were age ≥ 18 years and ability to provide informed consent. No exclusion criteria were defined. Primary end-point of the study is the occurrence of MACE (death, myocardial infarction, stent thrombosis, unplanned hospitalization for unstable angina, target lesion revascularization). Secondary end-points include individual components of MACE, procedural complications (periprocedural MI, bleedings, access site complication, failure to cross stent struts with guidewire in the treatment of bifurcation, failure to delivery the stent, contrast-induced nephropathy), bleedings at follow up.

NCT ID: NCT02772393 Recruiting - Schizophrenia Clinical Trials

A Study of Transition to the Paliperidone Palmitate 3-Month Formulation In Participants With Schizophrenia Previously Stabilized on the Paliperidone Palmitate 1-Month Formulation

Start date: April 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to estimate the proportion of participants fulfilling criteria for symptomatic remission following a transition to 12 months treatment with flexible-dose paliperidone palmitate 3 month formulation (PP3M) in participants with schizophrenia previously adequately treated with paliperidone palmitate 1 month formulation (PP1M) for at least 4 months.

NCT ID: NCT02699645 Recruiting - Hypertension Clinical Trials

Triple Therapy Prevention of Recurrent Intracerebral Disease EveNts Trial

TRIDENT
Start date: September 28, 2017
Phase: Phase 3
Study type: Interventional

An investigator initiated and conducted, multicentre, international, double-blinded, placebo-controlled, parallel-group, randomised controlled trial to determine the effect of more intensive blood pressure control provided by a fixed low-dose combination blood pressure lowering pill ("Triple Pill") strategy on top of standard of care, on time to first occurrence of recurrent stroke in patients with a history of stroke due to intracerebral haemorrhage.

NCT ID: NCT02649452 Recruiting - Healthy Clinical Trials

Acute Effects of Vibration on Shoulder Flexibility - Experimental Controlled Trial

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

Whole body vibration (WBV) can help to improve muscle flexibility by stimulating the neuromuscular functions. But there is a dearth in the literature to prove its effectiveness in improving the flexibility of the upper limb muscles. Therefore the purpose of the study is to determine the effects of vibration on improving upper limb flexibility. This experimental research will be conducted by recruiting participants at the age of 19 to 27 with no histories of injuries on the upper limb. They will be randomly assigned into two groups; experimental (with vibration) and control (no vibration) group. The WBV machine will be used to provide vibration to the upper extremities by placing both palms on the vibration platform. The outcome measure of active chest flexibility and shoulder reach flexibility will be performed pre and post vibration.

NCT ID: NCT02648945 Recruiting - Aerobic Exercise Clinical Trials

Effects of Low and High Intensity Exercise in Improving Working Memory Among Students With Anxiety Symptoms

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

Anxiety levels among the younger generation especially students have been increasing drastically in recent years. This severely affects a student's academics as previous studies have shown a strong correlation between high anxiety levels and poor working memory. Working memory, also known as short term memory is an important component in studying as it aids in holding important information needed to understand following information for a short period of time. This concerning phenomenon has drawn the attention of researchers to find solutions to this issue where recent studies have found physical exercise to contribute in the improvement of cognition which also includes working memory. Hence, the aim of this study is to compare the effects of low and high intensity exercises on working memory among students with high anxiety levels. Thirty female undergraduate students from UTAR with relatively high levels of anxiety will be conveniently sampled using Beck Anxiety Inventory. Participants will then be randomly allocated into 2 groups to undergo low and high intensity exercise on a treadmill according to Balke's Protocol. 2 memory assessments involving Verbal Memory Task will be conducted for each participant before and after the intervention.