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NCT ID: NCT04312464 Enrolling by invitation - COVID-19 Clinical Trials

Myocardial Damage in COVID-19

Start date: January 1, 2020
Phase:
Study type: Observational

This study aims to investigate the clinical characteristics, the incidence of myocardial injury, and the influence of myocardial injury on the prognosis in COVID-19 patients. There is no additional examination and treatment for this project.

NCT ID: NCT04308317 Enrolling by invitation - Clinical trials for Corona Virus Disease 2019,COVID-19

Tetrandrine Tablets Used in the Treatment of COVID-19

TT-NPC
Start date: March 5, 2020
Phase: Phase 4
Study type: Interventional

The study is expected to treat patients with mild and severe neo-coronary pneumonia through standard treatment regimens in combination with tetrandrine tablets, thereby reducing the clinical progress of some patients, improving prognosis, reducing the incidence of pulmonary fibrosis during rehabilitation, and improving patients' quality of life.

NCT ID: NCT04302636 Enrolling by invitation - Clinical trials for Refractory Schizophrenia

The Synergistic Effect of Hypoglycemic Index Diet on Refractory Schizophrenia

Start date: September 24, 2019
Phase: N/A
Study type: Interventional

This experiment was conducted to investigate the improvement of hypoglycemic index diet (LGIT) as a potential new intervention scheme for treatment-resistant schizophrenia, and to further explore the mechanism of efficacy.

NCT ID: NCT04259853 Enrolling by invitation - Clinical trials for ST Elevation Myocardial Infarction

Quantitative Fractional Ratio-guided Revascularization in STEMI Patients With Multi-vessel Disease

Start date: January 30, 2020
Phase: N/A
Study type: Interventional

About half of patients with ST-segment elevation myocardial infarction (STEMI) have multi-vessel lesions (> 50% diameter stenosis). But how to deal with the non-culprit vessels is still controversial. Previous studies have shown that flow fractional reserve (FFR)-guided revascularization on non-culprit vessels can further improve prognosis of such patients. However, FFR requires the use of pressure guidewire and special drugs such as adenosine to maximize induction of hyperemia forcoronary artery, which will increase the cost of operation and may cause additional risks. Quantitative flow ratio (QFR) is a novel angiography-based method for deriving FFR without pressure wire or induction of hyperemia. In present, there still are poor data about QFR-guided revascularization on non-culprit vessels in patients with STEMI. The purpose of this study is to compare the clinical effects of QFR-guided with angiography-guided revascularization on non-culprit vessel in STEMI patients with multi-vessel lesions.

NCT ID: NCT04253054 Enrolling by invitation - Clinical trials for Cardiovascular Diseases

Chinese Multi-provincial Cohort Study-Beijing Project

CMCS-Beijing
Start date: September 7, 2020
Phase:
Study type: Observational

The Chinese Multi-provincial Cohort Study (CMCS)-Beijing project is a sub-study in CMCS participants from Beijing, which intended to investigate the progression and determinants of atherosclerosis and aging related health problems through repeat examinations. Exam 0 to Exam 3 have been conducted during 1992 to 2012. Exam 4 is scheduled in 2020.

NCT ID: NCT04237844 Enrolling by invitation - Clinical trials for Bronchopulmonary Dysplasia

Clinic Features and Outcome of BPD (SGBPD)

Start date: December 1, 2020
Phase:
Study type: Observational

This study described the perinatal high-risk factors and clinical manifestations of the children, and compared the high-risk factors, clinical manifestations and prognosis of BPD among different clinical subtypes by comparison between groups. BPD grading was performed using the 2018 grading standard to compare the distribution of I/II/III BPD among different groups.

NCT ID: NCT04213742 Enrolling by invitation - Clinical trials for Patients ; Spinal Cord Injury

Study on the Application of Gratitude Intervention in Patients With Spinal Cord Injury

Start date: January 2, 2019
Phase: N/A
Study type: Interventional

To analyze the present situation and influencing factors of gratitude level and quality of life of patients with spinal cord injury, and to explore the methods of Thanksgiving intervention for patients with spinal cord injury so as to provide scientific basis for improving the quality of life of patients with spinal cord injury. Investigation and research design and experimental research design

NCT ID: NCT04210791 Enrolling by invitation - AL Amyloidosis Clinical Trials

Autologous Stem Cell Transplantation for Patients With AL Amyloidosis

Start date: July 1, 2010
Phase:
Study type: Observational [Patient Registry]

This study mainly evaluated the efficacy and safety of autologous stem cell transplantation for the treatment of AL amyloidosis, the role of induction and maintenance therapy in autologous stem cell transplantation, and the long-term efficacy and prognosis risk factors of autologous stem cell transplantation for the treatment of AL amyloidosis.

NCT ID: NCT04209959 Enrolling by invitation - Atrial Fibrillation Clinical Trials

Comparison of Efficacy and Safety of Different Doses of Nifekalant Instant Cardioversion of Persistent Atrial Fibrillation During Radiofrequency Ablation

Start date: January 1, 2019
Phase: Phase 4
Study type: Interventional

Atrial fibrillation (AF) is one of the most common tachyarrhythmias with substantial morbidity, disability and mortality. It is estimated that the number of patients with AF is expected to reach 7 million by 2050. Radiofrequency catheter ablation (RFCA) are the effective treatment for patients with drug-refractory symptomatic paroxysmal or persistent AF. However, the successful rate of RFCA for persistent AF during the first procedure still relatively low, the investigators also need pharmacological cardioversion or external electrical conversion. Several studies showed intravenous nifekalant injection after RFCA provided relative high rate of sinus conversion during catheter ablation in paroxysmal or persistent AF. Nevertheless, there is still no acceptable universal opinion on which dosage of nifekalant is preferable for converting AF during the operation. In order to address this issue, the investigators initiated the study to evaluate the efficacy and safety of different doses of intravenous nifekalant injection in the rapid cardioversion of persistent AF during radiofrequency catheter ablation.

NCT ID: NCT04208581 Enrolling by invitation - Clinical trials for Chronic Obstructive Pulmonary Disease

Yiqi Huoxue Huatan Granule for Reducing Mortality in COPD With Chronic Respiratory Failure

Start date: October 8, 2019
Phase: Phase 3
Study type: Interventional

This study aims to establish the treatment scheme of Yiqi Huoxue Huatan granule for chronic obstructive pulmonary disease (COPD) with chronic respiratory failure (CRF), reducing mortality, improving quality of life and forming high quality evidence.