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NCT ID: NCT03479424 Terminated - Clinical trials for Heart Failure With Reduced Ejection Fraction

Home Outpatient Monitoring and Engagement to Predict HF Exacerbation

Home Predict
Start date: October 8, 2018
Phase:
Study type: Observational

The HOME PREDICT HF study looks at new ways to predict hospitalizations for heart failure. We will use a set of devices at home and surveys to collect information about patient's health. This study uses the Eureka app, a new study app developed by the University of California, San Francisco. The study is designed to happen remotely, using this application on a patient's smartphone, so that is as convenient as possible to participate.

NCT ID: NCT03479125 Terminated - Liver Cirrhosis Clinical Trials

Post-Treatment Follow-up Study for Liver Disease Subjects With or Without Cirrhosis After Receiving Emricasan or Placebo

Start date: February 27, 2018
Phase:
Study type: Observational

A post-treatment follow-up observational study for liver disease subjects with or without liver cirrhosis after receiving emricasan or placebo. Subjects must have been enrolled in a prior IDN-6556 study to be eligible.

NCT ID: NCT03478293 Terminated - Clinical trials for Primary Open Angle Glaucoma (POAG)

iStent Inject in OAG Subjects on 2 Pre-op Topical Ocular Hypotensive Medications

Start date: February 27, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the intraocular pressure (IOP) lowering effect of iStent inject in eyes of subjects with primary open-angle glaucoma previously on two anti-glaucoma medications.

NCT ID: NCT03477526 Terminated - Clinical trials for Idiopathic Pulmonary Fibrosis and COPD

Status and Develepment Mental Quality of Life COPD/IPF Inpatients Before and After Pulmonary Rehabilitation

Start date: February 26, 2019
Phase: N/A
Study type: Interventional

As the result of our last study "Long Term effects of an Inpatient Pulmonary Program in Patients with Pulmonary Fibrosis" already demonstrated the positive effects of a Pulmonary Rehabiliation on the mental status. In this current study the aim will be to analyse the personality type regarding anxiety and depression

NCT ID: NCT03477474 Terminated - Clinical trials for Non-small Cell Lung Cancer Metastatic

Registry of Guardant360® Use and Outcomes In People With Advanced Cancer

GEODE
Start date: April 6, 2018
Phase:
Study type: Observational [Patient Registry]

The purpose of this registry is to collect data that describes the characteristics of people with advanced cancer for whom the Guardant360 assay is ordered and to observe their clinical outcomes after receiving their results.

NCT ID: NCT03476928 Terminated - Clinical trials for Uterine Fibroids and Heavy Menstrual Bleeding

A Study to Assess the Safety and Efficacy of Vilaprisan in Japanese Subjects With Uterine Fibroids and Heavy Menstrual Bleeding

ASTEROID 8
Start date: March 30, 2018
Phase: Phase 3
Study type: Interventional

To evaluate the safety and efficacy of vilaprisan in Japanese subjects with uterine fibroids and heavy menstrual bleeding (HMB).

NCT ID: NCT03475602 Terminated - Clinical trials for Idiopathic Membranous Nephropathy

Membranous Nephropathy-associated Serological Antibody Predict the Prognosis of Idiopathic Membranous Nephropathy

Start date: March 1, 2018
Phase:
Study type: Observational [Patient Registry]

Idiopathic membranous nephropathy (IMN) remains a common cause of the nephrotic syndrome in adults and one of the leading known causes of end-stage renal disease. Identification of circulating autoantigens provide potential biomarkers for diagnosis and therapy of idiopathic membranous nephropathy. M-type phospholipase A2 receptor (PLA2R) and Thrombospondin type-I domain-containing 7A (THSD7A) were identified as the target antigen in membranous nephropathy with high specificity and the concentration of serum anti-PLA2R antibody and anti-TSHD7A antibody were helpful for predicting disease activity. In our prospective cohort study, hospitalized patients diagnosed as IMN are prospectively studied. Circulating anti-PLA2R antibody and anti-THSD7A antibodies were recently screened by using enzyme-linked sorbent assay(ELISA). This study aims to analyse the difference of clinicopathological characteristics for different concentrations of serum anti PLA2R antibody and anti TSHD7A antibody, and analyze the association between baseline concentrations of serum antibody and disease activity. This study also explored the prediction effects of serum antibody concentrations with different types of therapeutic regimen in IMN and compare the curative effects of different types of therapeutic regimen in different serum antibody concentrations.

NCT ID: NCT03474432 Terminated - Clinical trials for Percutaneous Coronary Intervention

SOLEMN Study - Synergy Optical Coherence Tomography in Left Main PCI

SOLEMN
Start date: July 11, 2018
Phase: N/A
Study type: Interventional

BACKGROUD: Percutaneous coronary intervention (PCI) is increasingly used to treat unprotected left main coronary artery stenosis. Protected LM PCI is considered standard of care in most centers. OCT allows for precise determination of stent placement, stent expansion and apposition. The pattern of vessel healing can be very precisely studied if immediate post-stent implantation OCT/IVUS data is compared to the 6-month post-PCI interval. While OCT cannot be optimally used for ostial lesion imaging, IVUS can be used to image ostial lesions/stent placement. Optimal and consistent vessel healing is particularly important in LM PCI where stent thrombosis is a potential complication with serious adverse outcome. HYPOTHESIS: Due to the absorption of the polymer of the Boston Scientific Synergy Stent over time, early strut coverage patterns and timeline may be different than previously observed in DES and BMS stents in LM PCI. Late acquired stent malapposition (LASM) is expected to differ from previous observations with traditional DES/BMS. Stent coverage in LM PCI will be studied with OCT or IVUS at six and 12 months and compared to OCT or IVUS at the time of stent implantation. OCT/IVUS data will be analyzed in a core lab (CRF) and correlated with clinical outcomes at 6 and 12 months.

NCT ID: NCT03473496 Terminated - Clinical trials for Relapsed/Refractory Multiple Myeloma(MM)

CAR-T Cells Therapy in Relapsed/Refractory Multiple Myeloma

MM
Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Multiple myeloma(MM) is one of the most common malignant diseases in the blood system.There is still no cure for the disease which only control the development of the disease in various ways.Chimeric Antigen Receptor-transduced T cell (CAR-T) therapy is one of revolutionary targeted immunotherapy.The efficacy of CAR-T cells for the treatment of acute B lymphocytic leukemia has been widely recognized, and several clinical trials have been reported in the treatment of multiple myeloma with CAR-T cells.

NCT ID: NCT03473457 Terminated - Clinical trials for Relapsed/Refractory Acute Myeloid Leukemia(AML)

CAR-T Cells Therapy in Relapsed/Refractory Acute Myeloid Leukemia

AML
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

Acute myeloid leukemia (AML) is a group of genetically highly heterogeneous malignant disease . The disease is the most common type of adult acute leukemia. Overall survival (OS) was less than 50% in 5 years. Chimeric Antigen Receptor-transduced T cell (CAR-T) therapy is one of revolutionary targeted immunotherapy. The efficacy of CAR-T cells for the treatment of acute B lymphocytic leukemia has been widely recognized, although it start late, several clinical trials have been register in ClinicalTrials.gov.