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Drug Resistance clinical trials

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NCT ID: NCT02792816 Completed - Clinical trials for Plasmodium Falciparum Malaria

Molecular Surveillance of Artemisinin Resistance Malaria in Myanmar

Start date: June 2009
Phase: N/A
Study type: Observational

Efficacy and safety of the artemisinin combination therapy (ACT) in uncomplicated falciparum malaria patients in Myanmar and artemisinin molecular markers analysis

NCT ID: NCT02401204 Completed - Drug Resistance Clinical Trials

Bacterial Transmission Dynamics Study

BTS
Start date: February 2015
Phase:
Study type: Observational

Infections with multiply antibiotic-resistant bacteria represent a major cause of preventable morbidity and mortality amongst hospitalized neonates worldwide. In Southeast Asia, where antibiotic-resistance is a major problem, Gram-negative bacteria account for the majority of such infections. The most common pathogens are Acinetobacter spp., Pseudomonas aeruginosa, Enterobacter spp., Escherichia coli and Klebsiella pneumonia. The great majority of infections with these pathogens represent asymptomatic carriage, though in the absence of routine screening for asymptomatic carriage reliable estimates of the prevalence, rates of transmission between patients, and rates of importation from the community are lacking. Moreover, current understanding of the degree and manner in which different antibiotics act to select for such resistant organisms is rudimentary.

NCT ID: NCT01386476 Completed - Drug Resistance Clinical Trials

(18F)FCWAY and the Blood-Brain Barrier

Start date: June 15, 2011
Phase:
Study type: Observational

Background: - The blood-brain barrier helps protect the brain from infections and toxins in the blood stream. But it can also prevent certain drugs from reaching the brain to treat diseases or other problems. Researchers are interested in chemicals that will help show how the barrier works. One possible chemical, (18F)FCWAY, may be useful for studying the barrier. More tests are needed to determine how effective it is. Objectives: - To test whether (18F)FCWAY can be used to help study the blood-brain barrier. Eligibility: - Healthy volunteers between 18 and 50 years of age. Design: - This study requires a screening visit and two scanning visits. - Participants will be screened with a physical exam and medical history. They will also have blood and urine tests. - At the first scanning visit, participants will have a magnetic resonance imaging scan to provide baseline images of the brain. - Before the second visit, some participants will stay overnight in the hospital. They will receive the drug tariquidar, which may help the (18F)FCWAY show the blood-brain barrier more clearly. - At the second scanning visit, all participants will have a positron emission tomography scan with (18F)FCWAY to see how well the drug shows the blood-brain barrier on the scan.

NCT ID: NCT01039480 Completed - Drug Resistance Clinical Trials

Aspirin and Clopidogrel Resistance Study

Start date: May 2010
Phase: N/A
Study type: Observational

Resistance to antiplatelet drugs (aspirin, clopidogrel) is a recognized phenomenon with a prevalence from 17% to 35%. Resistance as detected by in vitro tests such as Multiple Electrode Aggregometry (MEA) has been shown to predict clinical therapy failure. Resistance can be caused by clinical, cellular and pharmacogenetic factors. Non compliance is suspected to be an important contributing factor. In this study, compliance will be assured with an electronical compliance monitoring system. Factors to non response will be identified to find plausible explanations when in vitro platelet aggregation inhibition is insufficient despite assured compliance. This study will help to disclose the relationship between compliance, biomarker and clinical outcome as well as to quantify the impact of non compliance to the resistance phenomenon as measured by MEA.

NCT ID: NCT00965042 Completed - Drug Resistance Clinical Trials

Effect of Ceftobiprole on Human Intestinal Microflora

Start date: April 2009
Phase: Phase 1
Study type: Interventional

The purpose of the study is to investigate the effect of ceftobiprole treatment on intestinal microflora in healthy volunteers.

NCT ID: NCT00563875 Completed - Drug Resistance Clinical Trials

Laboratory Aspirin Resistance in Diabetics and Non-Diabetics

Start date: November 2007
Phase: N/A
Study type: Interventional

Despite treatment with aspirin a large number of patients suffer a myocardial infarction. It has been speculated that these patients might be "resistant" to aspirin, and studies have indicated that this phenomenon is related to a less favourable prognosis. Furthermore, patients with diabetes mellitus have an increased risk of myocardial infarction and other vascular events and, recently, it has been suggested that diabetics do not respond adequately to aspirin. The purpose of this study is to compare the prevalence of "aspirin resistance" in diabetics and non-diabetics. Furthermore, patients who suffered a myocardial infarction while being treated with aspirin are included. We hypothesize that the prevalence of "aspirin resistance" will be higher among diabetics compared to other patients and to healthy individuals.

NCT ID: NCT00457236 Active, not recruiting - Clinical trials for Coronary Artery Disease

Effect of Clopidogrel Loading and Risk of PCI

EXCELSIOR
Start date: March 2003
Phase: N/A
Study type: Observational

This study is a prospective, single-center evaluation of the impact of the variability in platelet response after loading with clopidogrel on the peri-interventional risk of patients undergoing PCI.

NCT ID: NCT00389129 Completed - Drug Resistance Clinical Trials

Danish Aspirin Resistance Trial - Pilot Study

Start date: November 2006
Phase: N/A
Study type: Interventional

Despite treatment with aspirin a large number of patients suffer a myocardial infarction. It has been speculated that these patients might be "resistant" to aspirin, and studies have indicated that this phenomenon is related to a less favourable prognosis. At present, no international consensus exists on how to measure "aspirin resistance". The purpose of this study is to compare different methods for detecting "aspirin resistance". A classic but cumbersome way of evaluating platelet function will be compared to newer, easy-handling point-of-care tests. We hypothesize that one or more point-of-care tests will prove to be superior to the classic platelet function test in detecting aspirin resistance.

NCT ID: NCT00319150 Terminated - Clinical trials for Kidney Failure, Chronic

REPEAT Study - Resistance to ErythroPoietin Effectiveness Algorithm Trial

Start date: October 2006
Phase: Phase 3
Study type: Interventional

A strategy for optimizing erythropoietin therapy in patients with erythropoietin resistance. A multi-centered, open-label, randomized, controlled trial.

NCT ID: NCT00302913 Completed - Clinical trials for Coronary Artery Disease

Efficacy of Adjusted Clopidogrel Dose in Patients With Insufficient Platelet Inhibition

Start date: December 2005
Phase: N/A
Study type: Interventional

This study is a prospective, single-center evaluation of the efficacy of clopidogrel dose adjustment in patients with insufficient platelet inhibition after elective coronary stent implantation.