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NCT ID: NCT04811976 Recruiting - Clinical trials for Coronary Heart Disease

The Relationship Between Anxiety, Depression and Stent Restenosis After Percutaneous Coronary Intervention

Start date: December 1, 2019
Phase:
Study type: Observational

Percutaneous coronary intervention is currently one of the effective methods for the treatment of ACS. Unfortunately, the incidence of ISR is as high as 10%-20% at 3-6 months after PCI. So it is necessary to identify the potential risk factors to provide evidence for the prevention of ISR. Current research shows that anxiety and depression are related to the increased risk of major adverse cardiac events and mortality in patients with acute myocardial infarction. But there remains a relative paucity of evidence for the association between anxiety and depression and in-stent restenosis (ISR) .So a retrospective cohort study was conducted in the first hospital of Qinhuangdao in 2015-2020. The patients who underwent coronary angiography 1 year after PCI in our hospital from January 2015 to September 2020 were selected. Patients were divided into ISR and non-ISR groups depending on the follow-up coronary angiography results. Logistic regression model was utilized for analyzing the association of depression and anxiety with the in-stent restenosis (ISR) after PCI.

NCT ID: NCT04811651 Recruiting - Ischemic Stroke Clinical Trials

Umbilical Cord-derived Mesenchymal Stem Cells for Ischemic Stroke

UMSIS
Start date: March 15, 2021
Phase: Phase 2
Study type: Interventional

This is a doble blind, placebo controlled clinical trial to assess safety and efficacy of intravenous administration of Umbilical cord-derived Mesenchymal Stem cells in patients with ischemic stroke within 6 months of onset.

NCT ID: NCT04811586 Recruiting - Clinical trials for Multivessel Coronary Artery Disease

Efficacy and Safety of One-Stage Hybrid Coronary Revascularization

HCR-EAST
Start date: December 30, 2020
Phase: N/A
Study type: Interventional

Coronary revascularization could be accomplished either by percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG). PCI with drug-eluting stent (DES) implantation is featured by minimal invasive, low complication and rapid rehabilitation. CABG is characterized by improved long-term, event-free survival attributable to the use of left internal mammary artery (LIMA) graft. Hybrid coronary revascularization (HCR) consists of LIMA bypass to left anterior coronary descending artery (LAD) by minimal invasive direct coronary artery bypass (MIDCAB) and PCI of other stenosed coronary arteries with DES implantation. One-step HCR entails LIMA-LAD anastomosis performed through MIDCAB, immediately followed by PCI for non-LAD lesions, sometimes for diagonal branch, in the hybrid operating room. Limited data are available in comparing one-step HCR to PCI alone for the treatment of multivessel coronary artery disease(MVD). The current EAST-HCR study will investigate the efficacy and safety of one-step HCR for patients with MVD, as comparing to PCI alone.

NCT ID: NCT04810936 Recruiting - Malnutrition Clinical Trials

Early Nutritional Intervention in NPC Patients Undergoing Concurrent Chemoradiotherapy

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

This single center, open-label, randomized controlled clinical trial was designed to investigate whether early nutritional intervention with oral nutrition supplements in patients with nasopharyngeal carcinoma undergoing chemoradiotherapy will improve nutritional status, quality of life and treatment tolerance.

NCT ID: NCT04810910 Recruiting - Clinical trials for Resectable Pancreatic Cancer

Personalized Neoantigen Vaccine in Pancreatic Cancer Patients Following Surgical Resection and Adjuvant Chemotherapy

Start date: March 30, 2021
Phase: Phase 1
Study type: Interventional

This research study is evaluating a new type of pancreatic cancer vaccine called "Personalized Neoantigen Cancer Vaccine" as a possible treatment for pancreatic cancer patients following surgical resection and adjuvant chemotherapy. The purpose of the clinical study is evaluating the safety, tolerability and partial efficacy of the personalized neoantigen cancer vaccine in the treatment of resectable pancreatic cancer, so as to provide a new personalized therapeutic strategy. It is known that cancer patients have mutations (changes in genetic material) that are specific to an individual patient and tumor. These mutations can cause the tumor cells to produce proteins that appear very different from the body's own cells. It is possible that these proteins used in a vaccine may induce strong immune responses, which may help the participant's body fight any tumor cells that could cause the cancer to come back in the future. The study will examine the safety of the vaccine when given at several different time points and will examine the participant's blood cells for signs that the vaccine induced an immune response.

NCT ID: NCT04809909 Recruiting - Low Back Pain Clinical Trials

Peripheral Stimulation of Acupuncture Points for Low Back Pain

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

For decades, chronic low back pain has been one of the major health complaints in Hong Kong. Without proper management, low back pain is associated with functional disability and decreased quality of life. However, currently, there is still no "gold standard" treatment for cure of the problem.

NCT ID: NCT04809181 Recruiting - Clinical trials for Hematologic Malignancy

Azacitidine in Combination With Venetoclax Treatment for MRD Positive Post Allo-HSCT AML/MDS Patients

Start date: March 19, 2021
Phase: Phase 2
Study type: Interventional

In patients with MRD-positive patients after AML/MDS allogeneic hematopoietic stem cell transplantation, azacytidine combined with venetoclax may be effective in eliminating micro residual diseases, reducing the risk of relapse, and ultimately improving long-term survival.The primary purpose of this study was to explore an effective protocol to reduce the risk of relapse in patients with MRD positive after allogeneic hematopoietic stem cell transplantation for AML/MDS.

NCT ID: NCT04809142 Recruiting - Clinical trials for Advanced Biliary Cancer

A Study of TQB2450 Injection Combined With Anlotinib Hydrochloride Capsule as Second-line Treatment in Subjects With Advanced Biliary Cancer

Start date: February 4, 2021
Phase: Phase 3
Study type: Interventional

This study is a randomized, parallel controlled, multicentre phase III clinical trial to evaluate the efficacy and safety of TQB2450 combined with anlotinib versus chemotherapy as second-line treatment in subjects with advanced biliary cancer.

NCT ID: NCT04809025 Recruiting - Stomach Neoplasms Clinical Trials

Comparation of Endoscopic Biopsy and Postoperative Specimen for the Molecular Diagnosis of Gastric Cancer

EBPS
Start date: May 24, 2021
Phase:
Study type: Observational

This study aims to test the hypothesis that the diagnosis for histological type, histological grade, LAUREN type, HER-2 expression, MSI/dMMR status, and EBV status in gastric cancer is at least as reliable when performed on endoscopic biopsy specimens as on surgical resection specimens.

NCT ID: NCT04808856 Recruiting - Gout Clinical Trials

Treatment of Refractory Gout With ACTH or Methylprednisolone

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

To clarify the therapeutic effect and safety evaluation of ACTH in refractory gouty arthritis and special population, and to explore its mechanism of action.