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NCT ID: NCT02988531 Completed - Clinical trials for Coronary Artery Disease

Validation of PET-MRI for Cardiovascular Disease

Start date: February 9, 2017
Phase: N/A
Study type: Interventional

To determine whether PET-MRI can obtain comparable images to PET-CT in those with coronary artery disease.

NCT ID: NCT02868671 Completed - Clinical trials for Mild Traumatic Brain Injury

Acupuncture for Mild Traumatic Brain Injury:A Functional Magnetic Resonance Imaging Study

Start date: August 2016
Phase: N/A
Study type: Interventional

The overall goal of this study is to examine if acupuncture intervention can reduce the post-concussion symptom (PCS), and affective and cognitive complaints among mild traumatic brain injury (TBI). This study also hypothesized that compared to those in the sham acupuncture and waiting list control groups, patients in the real acupuncture group will have fewer symptoms of depression, sleep problems and post-concussion symptoms.

NCT ID: NCT02548819 Completed - MRI Clinical Trials

University Hospital Cardiac Device MR Registry: The Safety of MR Imaging in Patients With Implanted Cardiac Devices

CDMR
Start date: September 2015
Phase: N/A
Study type: Observational [Patient Registry]

A single-center registry to prospectively evaluate the safety of non-cardiac/non-thoracic magnetic resonance imaging (MRI) in patients with implanted cardiac devices (pacemakers and implantable cardioverter defibrillators).

NCT ID: NCT02200809 Completed - Prostate Cancer Clinical Trials

MR-guided Focal Laser Ablation of the Prostate

Start date: July 2014
Phase: N/A
Study type: Interventional

Purpose of the investigators study is to determine the short and medium term histological cancer control of focal therapy using MR-guided focal laser ablation therapy in the treatment of localised prostate cancer.

NCT ID: NCT01884987 Recruiting - Clinical trials for Nasopharyngeal Carcinoma

Treatment of Cerebral Radiation Necrosis With GM1, a Prospective Study

Start date: January 2012
Phase: Phase 2
Study type: Observational [Patient Registry]

Cerebral radiation necrosis (CRN) is a well-documented late complication of radiation therapy for cancers, and may have a devastating effect on the patient's quality of life (QOL). However,CRN was once regarded as a progressive and irreversible disease, no standard therapy has been suggested for CRN. In our clinical practice, we have used monosialotetrahexosylganglioside (GM1)to treat CRN, and found that GM1 can successfully reverse CRN. So we carried out this prospective study to test the efficacy of GM1 for CRN.

NCT ID: NCT01578694 Completed - MRI Clinical Trials

Characterization of Proteoglycan Depletion in Femoroacetabular Impingement With T1ρ Magnetic Resonance Imaging (MRI)

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

Magnetic resonance imaging (MRI) has proven to be one of the best ways to image articular cartilage. A tremendous amount of research has focused on cartilage imaging with an emphasis of early-osteoarthritis (OA) characterization. One of the techniques which has shown great promise is the imaging technique called T1ρ . The advantage of this pulse sequence is that it is sensitive to proteoglycans (PG), a major macromolecule degraded in OA. The study objective is to determine if T1ρ can acutely assess PG content in femoroacetabular impingement (FAI) which may allow physicians to differentiate between normal and early-OA cartilage states in FAI patients.

NCT ID: NCT01420211 Completed - Pharmacokinetics Clinical Trials

Influence of the OATP1B1 and OATP1B3 Genotype on the Hepatic Uptake of Primovist®

Start date: October 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The objective of the study is to assess the hepatic uptake of Primovist® after intravenous administration of 25 µmol/kg body weight in 56 healthy volunteers and in 60 patients with a liver disease in dependence on the OATP1B1- and OATP1B3-genotype.

NCT ID: NCT01277055 Recruiting - Myocardial Ischemia Clinical Trials

MRI Perfusion Imaging at 3Tx Compared to Invasive FFR Measurements

Vision MRT
Start date: January 2011
Phase: N/A
Study type: Observational

Coronary artery disease (CAD) has a great significance concerning prevalence and mortality in the western world. It is usually diagnosed by catheterization and coronary arteries are visually assessed by the examiner. Thus having a great spectrum of interobserver differences, especially when it comes to intermediate lesions. The gold standard to assess the haemodynamic significance is the measurement of the myocardial fractional flow reserve (FFR). The FAME-study (Tonino, De Bruyne et al. 2009) was able o show that additional FFR- measurements in patients with intermediate lesions could significantly reduce stent implementation and consequently mortality. However this method is not used in daily routine and is available only in a fraction of catheter labs worldwide. Taking this into account decision finding especially in intermediate lesions remains difficult. One major step to simplify the invasive approach concerning intermediate lesions would be to establish a non-invasive procedures which localizes the coronary vessel to intervene ahead catheterization. Do to steady technical development cardiac MRI has become a powerful tool which is able to determine myocardial vitality, perfusion and function. In particular the new generation of 3 Tesla multi transmit MR with its higher field strength and better spatial resolution seems to be able to show first pass myocardial perfusion more precise. With this new technology prefixed to cardiac catheterization clinical relevant information can be made accessible and thus reduce the number of unnecessary implemented stents.

NCT ID: NCT01168479 Completed - Prostate Cancer Clinical Trials

FLAME: Investigate the Benefit of a Focal Lesion Ablative Microboost in Prostate Cancer

FLAME
Start date: September 2009
Phase: Phase 3
Study type: Interventional

Rationale: Dose escalation in external-beam irradiation has proven to benefit outcome in local prostate cancer. Randomized trials were performed up to doses of 78 Gy in 2 Gy fractions. Nevertheless, the five-year biochemical relapse rate still was approximately 35% in the high-dose arm. Therefore further dose escalation seems to be required. A feasibility study up to appr. 85 Gy on the entire prostate has already been performed and showed acceptable toxicity when combined with adequate position verification. Higher doses to the entire prostate are expected to increase severe toxicity. As local recurrences only occur at the site of the primary macroscopic tumour area the next step in increasing the dose should be an ablative boost to the macroscopic tumour alone, while electively irradiating the rest of the prostate to the current gold standard dose. Feasibility of this approach has been shown for an ablative dose of 95 Gy to the macroscopic tumour within the prostate.

NCT ID: NCT01160471 Completed - MRI Clinical Trials

Noninvasive Imaging of Heart Failure: A Pilot Study

Start date: July 1, 2010
Phase:
Study type: Observational

Background: - Heart failure is a common cardiovascular disorder whose incidence increases with age, affecting up to 10% of people older than 65 years of age. As the population ages, the prevalence and cost of heart failure will continue to rise. Researchers are interested in using noninvasive imaging methods to better understand the symptoms and effects of heart failure. Objectives: - To conduct a noninvasive comparative imaging study of individuals with heart failure. Eligibility: - Individuals at least 18 years of age who have been diagnosed with heart failure (with at least mild symptoms and slight limitations on physical activity). Design: - This study will last approximately 2 years and will require four visits to the National Institutes of Health Clinical Center, with one screening visit and three study visits. - Participants will be screened with a full medical history and physical examination, as well as blood and urine samples. - Participants will have the following tests during each study visit: - Physical examination - Blood and urine samples - Cardiac magnetic resonance imaging - Cardiac computerized tomography to study the blood vessels in and leading to the heart - Echocardiogram to evaluate heart function - Electrocardiogram to measure heart electrical activity - The three study visits will take place 1 year apart. Participants will also receive follow-up phone calls 6 months after the first and second visits. - No treatment will be provided as part of this protocol.