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NCT ID: NCT02469441 Completed - Postoperative Ileus Clinical Trials

Does Coffee Intake Reduce Postoperative Ileus After Elective Colorectal Surgery

COFFEE
Start date: August 1, 2014
Phase: N/A
Study type: Observational

The aim of the study is to investigate if postoperative coffee intake decreases the time until first bowel movement in elective colorectal surgery with primary anastomosis.

NCT ID: NCT02469376 Terminated - Clinical trials for Deep Vein Thrombosis

Evaluation of a New Imagingtechnologie for Thrombosis

PET-GP1_1
Start date: September 2014
Phase: Phase 1
Study type: Interventional

Arterial and venous thrombi play an important role in various vascular diseases such as myocardial infarction, stroke, transient ischemic attacks (TIA) and pulmonary embolism. These thromboembolic disorders are the leading causes of morbidity and mortality worldwide. A non-invasive method for the quantitative and effective detection of thrombi in the whole body has not yet been established. In spite of the available techniques, 30% to 40% of ischemic strokes "cryptogenic" (undetermined cause, the source of thromboembolism is never identified). Possible causes of cryptogenic stroke atherosclerosis include in the aortic arch or intracranial arteries. A plaque in the arch or other large vessels could be an important source of cryptogenic strokes, however, are those difficult to detect by routine methods. The approach of thrombus targeted molecular imaging could identify potentially troublesome plaques early on before they become a dangerous rupture. The hypothesis is that the radiotracer 18F-arterial GP1 and venous thrombi using positron emission tomography (PET) can be made visible. The primary goal is the potential applicability of the substance as a PET tracer for diagnosing thrombi.

NCT ID: NCT02469051 Completed - Clinical trials for Coronary Artery Disease

Breath-hold Cardiac Hybrid SPECT/CCTA

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

This study aims at combining inspiration breath-hold myocardial perfusion SPECT with coronary CT angiography.

NCT ID: NCT02468960 Active, not recruiting - Clinical trials for Coronary Artery Disease

Optimal Lesion Preparation With Non-compliant Balloons Before Implantation Of Bioresorbable Scaffolds (OPreNBiS)

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

Study aim : To compare a novel strategy of lesion preparation with noncompliant balloons before implantation of BVS (Bioresorbable Vascular Scaffold). Hypothesis: Predilatation with non-compliant balloons could facilitate optimal deployment of BVS. By achieving good scaffold apposition a need for post-dilatation could be significantly reduced. This is expected to result in better short- and long-term outcomes.

NCT ID: NCT02468869 Completed - Clinical trials for Information Structuring Skills

Improving Discharge Communication in the Emergency Department Through Information Structuring

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

The goal of the proposed study is to assess the potential of information structuring for improving discharge communication. Specifically, the investigators aim to examine the advantages of an information-structuring skills training for physicians (compared to an empathy skills training) on discharge communication and associated patient outcomes, such as patients' information recall and adherence to physician recommendations. The investigators hypothesize that patients receiving structured discharge information from their trained physicians will be able to recall more information and show higher adherence to recommendations relative to controls (i.e., patients receiving discharge information from doctors trained in empathy skills).

NCT ID: NCT02468674 Completed - Sarcopenia Clinical Trials

A 24-week Off-drug Extension Study in Sarcopenic Elderly Who Completed Treatment in the 6-month Core Study

Start date: July 22, 2015
Phase: Phase 2
Study type: Interventional

This extension study was a 24-week off-drug follow-up of the core CBYM338E2202 (NCT ) study and the main objective was to determine the long-term durability of bimagrumab (BYM338) effect after a 6-month treatment period.

NCT ID: NCT02468609 Recruiting - Pulmonary Emphysema Clinical Trials

Diagnostic Value of Ultralow-dose Computed Tomography for the Detection of Pulmonary Nodules and Lung Parenchym Alterations Compared to Standard-dose CT

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

To investigate the diagnostic value of ultralow-dose computed tomography in the detection of pulmonary nodules and lung parenchym alterations (e.g. emphysema) compared to standard-dose-CT.

NCT ID: NCT02467621 Completed - Clinical trials for Gastrointestinal Bleeding

Stress Ulcer Prophylaxis in the Intensive Care Unit

SUP-ICU
Start date: January 2016
Phase: Phase 4
Study type: Interventional

Stress ulcer prophylaxis (SUP) is standard of care in the intensive care unit (ICU), however the quantity and quality of evidence is low and potential harm has been reported. The aim of the SUP-ICU trial is to asses the overall benefits and harms of SUP with proton pump inhibitor in adult critically ill patients in the ICU.

NCT ID: NCT02467582 Active, not recruiting - Colon Cancer Clinical Trials

Adjuvant Aspirin Treatment for Colon Cancer Patients

Start date: June 9, 2016
Phase: Phase 3
Study type: Interventional

Following complete resection of their primary tumor, potentially eligible stage II or stage III colon cancer patients will undergo central PIK3CA testing. Patients with somatic mutations will be 2:1 randomized to daily aspirin 100 mg versus placebo for a a maximum of 3 years or until disease recurrence, patient death or withdrawal of consent, whichever occurs first. Patients will be followed up for at least 3 years from the date of surgery. The intake of aspirin or placebo is independent of adjuvant chemotherapy, and does not impact on the indication to give (or not to give) adjuvant chemotherapy.

NCT ID: NCT02467270 Active, not recruiting - Clinical trials for Myeloid Leukemia, Chronic, Chronic Phase

Ponatinib in Participants With Resistant Chronic Phase Chronic Myeloid Leukemia (CP-CML) to Characterize the Efficacy and Safety of a Range of Doses

OPTIC
Start date: June 30, 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to characterize the efficacy of ponatinib administered in 3 starting doses (45 mg, 30 mg, and 15 mg daily) in participants with CP-CML who are resistant to prior tyrosine-kinase inhibitor (TKI) therapy or have T315I mutation, as measured by <=1 % Breakpoint Cluster Region-Abelson Transcript Level using International Scale (BCR-ABL1IS) at 12 months.