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Chest Pain clinical trials

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NCT ID: NCT02170103 Completed - Chest Pain Clinical Trials

Microvascular Recovery With Ultrasound in Myocardial Infarction (MRUSMI) Post PCI Trial

MRUSMI
Start date: September 16, 2018
Phase: N/A
Study type: Interventional

The investigators propose to test the effectiveness of a technique that uses a modified commercially available ultrasound system used for cardiac imaging, and a commercially available ultrasound contrast agent (microbubbles) to break up the blood clots that cause heart attacks. The ultrasound and microbubbles will be applied as soon as possible to patients presenting to the emergency department, after an EKG confirms that a heart attack is ongoing. Patients who provide emergent consent will be randomized to either conventional therapy for a heart attack, or conventional therapy and ultrasound with microbubbles. The ultrasound will be applied both before and after emergent heart catheterization, in order to break up the blood clots that are not only in the artery supplying the heart muscle, but also in the small branches (capillaries) that are fed by this artery. Following the randomized treatment, patients will be followed for the development of any complications (recurrent heart attack, heart failure, or need for defibrillator placement) as well as by echo and cardiac MRI to determine how much heart muscle was salvaged by the treatment.

NCT ID: NCT02144090 Completed - Chest Pain Clinical Trials

Opsens Optowire for Fractional Flow Reserve - The O2 Pilot Study

O2
Start date: May 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the usability and safety of the Opsens OptoWire and Optomonitor in measuring fractional flow reserve (FFR) in patients with coronary artery disease who are undergoing a coronary angiogram.

NCT ID: NCT02116426 Completed - Chest Pain Clinical Trials

Copeptin Testing During Pre-hospital Care in the Treatment of Chest Pain Suggestive of Acute Coronary Syndrome

SCA COP
Start date: July 29, 2015
Phase: N/A
Study type: Observational

The main objective of our study is to evaluate the diagnostic value of copeptin testing in association with troponin HS testing during pre-hospital care (ambulance care) in the treatment of patients whose pattern of use is the occurrence chest pain suggestive of ACS but not ST+.

NCT ID: NCT02107001 Completed - Lung Cancer Clinical Trials

Lung Ultrasound in Pleuritic Chest Pain

UPP
Start date: March 2014
Phase: N/A
Study type: Observational

Chest pain is an alarming symptom and one of the most frequent causes of access to the Emergency Departement. Although chest X-ray remains an essential step in the diagnostic process, several studies showed numerous limitations of radiography which frequently is inconclusive. Ultrasonography is a non-radiating imaging technique. Albeit a wide use of ultrasound, the utilization of ultrasound in the study of the lung has only recently been introduced in the clinical practice. Several studies proved that lung ultrasound is useful in the diagnosis of lung consolidation in community acquired pneumonia. Nowadays, ultrasound is not routinely used in the presence of chest pain. Our hypothesis based on clinical experience is that, in patients with pleuritic chest pain, lung ultrasound is very sensitive in detecting pneumonia and other lung diseases (such as pneumothorax) thus performing better than radiography. The primary aim of this study is to verify, in patients affected by pleuritic chest pain, the accuracy of lung ultrasound compared to chest-X-ray. The secondary aim is to evaluate the accuracy of lung ultrasound consolidations in distinguishing lung consolidation in pneumonia, atelectasis, pulmonary infarction, or tumors.

NCT ID: NCT02056964 Completed - Clinical trials for Acute Coronary Syndrome

HEART Pathway Implementation

Start date: November 2013
Phase:
Study type: Observational

The purpose of this study is to determine the effectiveness of the HEART Pathway, a clinical decision aid for the care of patients with chest pain, in a "real-world" clinical setting. This will be accomplished through the building of a transformative collaboration between research, education, and health systems operations to more effectively and efficiently provide patient care.

NCT ID: NCT02055443 Completed - Chest Pain Clinical Trials

Myocardial Ischemia Detection for Early Identification of Patients With Ischemic Chest Pain

MID-EPIC
Start date: January 2014
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate whether new novel markers from the clinical electrocardiogram (EKG), which have been used as non-invasive measures of heart disease, can detect coronary artery disease in patients with chest pain. The researchers are especially interested in studying how changes in these unique waves evolve over time with rest and activity. It is hoped that the findings will be helpful in differentiating patients with cardiac chest pain at emergency departments from those with non-cardiac chest pain, as early identification can accelerate treatment and save lives. Eligible participants are those age 18 and older who have been referred for a nuclear stress test at University of Pittsburgh Medical Center Presbyterian Hospital to rule out coronary artery disease as part of their clinical care.

NCT ID: NCT02042209 Completed - Clinical trials for Acute Coronary Syndrome

Medical Telephone Triage of Emergency Calls for Thoracic Pain

DOREMI2
Start date: May 2010
Phase:
Study type: Observational

Thoracic pain is the main symptom of acute coronary syndrome (ACS), urgent and serious illness. Whereas hospital mortality decreased until reaching 10%, out-of-hospital mortality remains high: half of the deaths occur during the first two hours. The benefit of an early diagnosis of ACS in term of morbidity and mortality is well established. Identification of the coronary origin of a thoracic pain by the telephone triage physician of the pre-hospital emergency service (SAMU) leads to the sending of a physician staffed ambulance (UMH) and is thus a key element of the prognosis. The aim of the study is to build a telephone predictive score of ACS at the triage of calls for non traumatic thoracic pain. The separate analysis of the questionnaires by sex will authorize the validation of a unique score or two distinct scores for men and women.

NCT ID: NCT02031016 Completed - Chronic Pain Clinical Trials

Remifentanil vs Fentanyl During Cardiac Surgery and Chronic Thoracic Pain

REFLECT
Start date: February 2014
Phase: Phase 4
Study type: Interventional

This study will investigate the influence of intra-operative use of remifentanil versus fentanyl on the percentage of patients with chronic thoracic after cardiac surgery via sternotomy. Secondary quantitative sensory testing is performed to determine thermal and electrical detection and pain threshold and the difference in pain variability scoring. Postoperative pain scores, analgesic use, genetic variances and costs are measured.

NCT ID: NCT02015858 Completed - Chest Pain Clinical Trials

Pain During Chest Tube Withdrawal: Evaluation Using Pan Monitor

Pain Drain
Start date: June 2013
Phase: N/A
Study type: Observational

Pain evaluation remains a clinical problem. Pain Monitor allows pain evaluation using the measurement of skin conductance. Withdrawal of chest tube can be painful and the purpose of the study was to compare auto-evaluation of pain (visual analogic scale) and the index measured by the Pain Monitor.

NCT ID: NCT02014311 Completed - Clinical trials for Coronary Artery Disease

CArdiac cT in the Treatment of Acute CHest Pain 2 - Myocardial CT Perfusion

CATCH2
Start date: October 2013
Phase: N/A
Study type: Interventional

The aim of this study is to assess whether the clinical management of patients with recent acute-onset chest pain without acute coronary syndrome may be optimized by a combined coronary CT angiography (CTA) + CT myocardial perfusion (CTP) guided, rapid diagnostic strategy as compared to CTA alone. CT diagnostic evaluation and potential referral for invasive testing will be performed within 2 weeks after hospital discharge. The following main hypothesis will be tested: - Combined assessment of coronary anatomy and myocardial perfusion using 320 MDCT results in a safe and optimized, cost-effective invasive treatment strategy