Clinical Trials Logo

Acute Disease clinical trials

View clinical trials related to Acute Disease.

Filter by:

NCT ID: NCT03892694 Active, not recruiting - COPD Clinical Trials

Metered Cryospray for the Treatment of Patients With Chronic Obstructive Pulmonary Disease With Chronic Bronchitis

Start date: February 14, 2020
Phase: N/A
Study type: Interventional

To evaluate the relationship between airway structure and function in patients with chronic bronchitis treated with metered cryospray (MCS).

NCT ID: NCT03834961 Active, not recruiting - Solid Neoplasm Clinical Trials

Larotrectinib in Treating Patients With Previously Untreated TRK Fusion Solid Tumors and TRK Fusion Relapsed Acute Leukemia

Start date: October 25, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects and how well larotrectinib works in treating patients with previously untreated TRK fusion solid tumors and TRK fusion acute leukemia that has come back. Larotrectinib may stop the growth of cancer cells with TRK fusions by blocking the TRK enzymes needed for cell growth.

NCT ID: NCT03832257 Completed - Acute Disease Clinical Trials

Improving Safety of Transitions to Skilled Nursing Care Using Videoconferencing

ECHO-CT
Start date: September 30, 2018
Phase: N/A
Study type: Interventional

This prospective cohort study seeks to determine if the ECHO-CT program, a healthcare videoconferencing program, can improve clinical outcomes while reducing cost and resource utilization when expanded to a community hospital setting. Data will be analyzed on the facility level and patient level.

NCT ID: NCT03827590 Recruiting - Acute Bronchitis Clinical Trials

Clinical Trials to Assess the Efficacy and Safety of HLIM

Start date: November 29, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of HLIM

NCT ID: NCT03797651 Recruiting - Clinical trials for Coronary Artery Disease, Acute Coronary Syndrome

Ticagrelor Monotherapy in PAtients Treated With New-generation Drug-eluting Stents for Acute Coronary Syndrome; T-PASS Trial

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

We hypothesized that ticagrelor monotherapy might be enough to prevent thromboembolic events without aspirin after PCI in patients with acute coronary syndrome(ACS). Moreover, ticagrelor monotherapy will reduce bleeding risk compared to DAPT with aspirin plus ticagrelor. We will also evaluate 1-year safety and efficacy of Orsiro stent for patient with acute coronary syndrome. After confirmation of enrollment, patients will be randomized to continue standard treatment (aspirin plus ticagrelor) for 1 year or to stop aspirin after discharge or less than 1 month after PCI (ticagrelor monotherapy). Randomization will be stratified according to 1) the presence of diabetes and 2) ST elevation myocardial infarction (MI). Baseline clinical and angiographic characteristics, laboratory findings will be assessed at the time of randomization. All patients will provide informed consent on their own initiative.

NCT ID: NCT03779854 Recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Naive T Cell Depletion for Preventing Chronic Graft-versus-Host Disease in Children and Young Adults With Blood Cancers Undergoing Donor Stem Cell Transplant

Start date: August 29, 2019
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well naive T-cell depletion works in preventing chronic graft-versus-host disease in children and young adults with blood cancers undergoing donor stem cell transplant. Sometimes the transplanted white blood cells from a donor attack the body's normal tissues (called graft versus host disease). Removing a particular type of T cell (naive T cells) from the donor cells before the transplant may stop this from happening.

NCT ID: NCT03756675 Recruiting - Acute Leukemia Clinical Trials

Haploidentical Peripheral Blood Stem Cell Transplantation for Acute Leukemia

Start date: November 1, 2018
Phase:
Study type: Observational

Allogeneic stem cell transplantation (Allo-HSCT) is the effective and even the only treatment for hematological malignancies. The "GIAC" protocol established by our center has successfully crossed the HLA barrier in HLA-mismatched/haploidentical HSCT. The protocol entails the following: treating donors with granulocyte colony-stimulating factor (G-CSF) to induce donor immune tolerance, intensified immunologic suppression to both promote engraftment and to prevent GVHD, antithymocyte globulin (ATG) was included for the prophylaxis of GVHD and graft rejection, and combination of G-CSF-primed bone marrow harvest (G-BM) and G-CSF-mobilized peripheral blood stem cell harvest (G-PB) as the source of stem cell grafts. But peripheral blood transplantation is still prevalent. Compared with BM, G-PB is more convenient to collect, and the number of T lymphocytes and CD34+ cells is higher. It is reported that G-PB has a higher implantation rate and even a higher disease-free survival rate in sibiling-identical transplantation compared with BM transplantation, whereas there were also reports with different conclusions. This prospective, one-arm clinical cohort study aims to evaluate the safety and efficacy of haplotype peripheral blood stem cell transplantation (PBSCT) in the treatment of acute leukemia.

NCT ID: NCT03754777 Completed - Acute Appendicitis Clinical Trials

Modified Enhanced Recovery Program in Emergency Surgery (MERES)

MERES
Start date: July 1, 2017
Phase: N/A
Study type: Interventional

Laparoscopic appendectomy (LA) is a widespread surgical procedure. Patients may develop considerable postoperative pain and dyspepsia resulting in prolong in-hospital stay. Almost 10% of patients develop postoperative complications. Enhanced recovery after surgery (ERAS) program has proven its effectiveness in elective surgery and can theoretically improve outcomes of LA. To date there is no ERAS program for LA. The aim of the study was to investigate the safety and efficacy of a modified ERAS protocol in LA.

NCT ID: NCT03754023 Completed - Acute Kidney Injury Clinical Trials

Biomarker Rule in/Out in Patients With Acute Diseases for Validation of AKI (BRAVA) Acute Kidney Injury

BRAVA
Start date: November 1, 2018
Phase:
Study type: Observational

The presence or development of AKI impacts on outcomes in patients presenting with acute conditions to the ED. As a result, treating physicians are often concerned with the risk of AKI and take such risk in consideration when making subsequent therapeutic and diagnostic decisions which may result in delaying or withholding therapeutic measures in order to prevent further kidney damage (i.e. avoid imaging studies with contrast media). If clinicians could be informed early that a patient is at minimal risk for AKI, they could deploy timely and optimal diagnostic and treatment procedures for the underlying disease of the patient without major concerns for causing or exacerbating kidney damage

NCT ID: NCT03743909 Not yet recruiting - Acute Leukemia Clinical Trials

Expression of Aberrant CD Markers in Acute Leukemia:Retrospective Study in South Egypt Cancer Institute

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

- To determine incidence of Expression of aberrant CD markers in acute leukemia in South Egypt . - Correlation between this expression and outcome of the patient.