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NCT ID: NCT03534921 Completed - Clinical trials for Diabetes Mellitus, Type 2

Improving Diabetes Outcomes for People With Severe Mental Illness (SMI)

EMERALD
Start date: April 1, 2018
Phase:
Study type: Observational

This study aims to identify the determinants of diabetes and to explore variation in diabetes outcomes for people with severe mental illness (schizophrenia, schizoaffective disorder and bipolar disorder) in order to develop potential healthcare interventions that can be tested further. The study utilises a mixed methods design comprising analysis of patient primary care records and interviews with patients living with comorbid SMI and diabetes, family carers and healthcare professionals involved in commissioning or delivering healthcare for this population. This entry on the Protocol Registration and Results System describes only the quantitative Work Package of the study in detail i.e. analysis of patient primary care records.

NCT ID: NCT03537430 Completed - Mediastinal Tumor Clinical Trials

Totally no Tube (TNT) Uniportal Video-assisted Thoracoscopic Surgery (VATS) VS Traditional Uniportal VATS for Mediastinal Tumor

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

TNT surgery is a new area of exploration and evolution in thoracic minimal invasive surgery. TNT Uniportal Video-assisted Thoracoscopic Surgery (VATS) has become popular during mediastinal tumors resection. However, there has been little randomized controlled trials into the associated feasibility and advantage. The aim of our RCT was to evaluate the feasibility and advantage of TNT Uniportal VATS for mediastinal tumors resection and its significance in Fast Track Surgery (FTS). This is a single-center prospective randomized controlled trial. 98 patients aged between 18 and 75 years with clinically mediastinal tumors were randomly assigned to two groups, 50 patients received TNT uniportal VATS mediastinal tumor resection (TNT group) and 48 patients underwent traditional uniportal VATS mediastinal tumor resection (control group), the short-term perioperative outcomes would be reported here.

NCT ID: NCT03539783 Completed - Clinical trials for Respiratory Distress Syndrome

Identifying PARDS Endotypes

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

Pediatric acute respiratory distress syndrome (PARDS) is a severe and diffuse lung injury that is a common cause of admission and mortality in the pediatric intensive care unit (PICU). PARDS can be secondary to many different causes, and there are few therapies that have been shown beneficial in PARDS. This study seeks to identify important PARDS subtypes using gene expression profiling of bronchial epithelial cells from control and PARDS subjects.

NCT ID: NCT03542201 Completed - Clinical trials for Health Knowledge, Attitudes, Practice

Comparison of Blogshot Formats With Standard Cochrane Plain Language Formats

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

Participants will receive in random order on format of brief description of systematic review summary on health intervention. One group will receive standard plain language summary, while another will receive Cochrane blog shot, containing only few information about the efficacy of the intervention. After reading, their task will be to answer several questions about the material they have read.

NCT ID: NCT03544203 Completed - Clinical trials for Intraabdominal Infections

Multicentre Observational Study on Community Acquired Intraabdominal Infections Management

PERICOM
Start date: April 1, 2018
Phase:
Study type: Observational

Intraabdominal infection require rapid care management including antibiotic therapy and source control. Morbidity and mortality associated with Intraabdominal infections remain high. French recommendations have been edited in 2000 further updated in 2014. Delay in diagnosis and surgery can lead to worsened outcomes. However, little data are available on early community-acquired intraabdominal infections management to identify risk factors of inadequate management.

NCT ID: NCT03545178 Completed - Diabetes Mellitus Clinical Trials

Systematic Evaluation of Continuous Glucose Monitoring Data

SECOND
Start date: April 1, 2018
Phase:
Study type: Observational

This study retrospectively evaluates continuous glucose monitoring (CGM) and flash glucose monitoring (FGM) data and pursues two main objectives: First, the investigators analyze if glucose values are better controlled in the days directly before a consultation at our tertiary referral centre (so called "white coat adherence"). Second, the investigators use the collected CGM and FGM data to develop a hypoglycemia prediction model.

NCT ID: NCT03545763 Completed - Hypertension Clinical Trials

Evaluating Control of Hypertension - Effect of Social Determinants

ECHOES
Start date: April 1, 2018
Phase:
Study type: Observational

This study evaluates the impact of a large-scale, national expansion of Medicaid on hypertension incidence, screening, treatment, and management. Social Determinants of Health will be assessed as moderators, and comparing states that did versus states that did not expand Medicaid will also be evaluated.

NCT ID: NCT03546114 Completed - Gender Role Clinical Trials

Does Gender Matter? Patient Preference in an Italian Osteopathic Clinical Setting

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

This study evaluates patients preference for the gender of their osteopath. All patients referring to an Italian private osteopathic clinic will receive a proper questionnaire before knowing the gender of their designed osteopath.

NCT ID: NCT03554252 Completed - Clinical trials for Health Knowledge, Attitudes, Practice

Comparison of Different Frames of Numerical Information in Cochrane Plain Language Summaries

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

Participants will be randomly given one of two formats containing descriptions of health interventions. In one format, participants will have to read short summaries where results of the intervention are presented as frequencies and the side effects of health intervention are presented as percentages, while in another format the frames will be reversed (results will be presented as percentages and side effects as frequencies). After reading, participants will be asked several questions about the content of the summary and its conclusions.

NCT ID: NCT03557892 Completed - Clinical trials for Diabetes Mellitus, Type 1

Sensor-augmented Pump Versus Multiple Daily Injections With Degludec as Basal Insulin for Insulin Therapy in Type 1 Diabetes

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

Several studies have shown that Continuous Subcutaneous Insulin Infusion together with Continuous Glucose Monitoring improves glycemic control in type 1 diabetes when compared to more traditional approaches; however, in available trials the basal insulin used in multi-injection therapy is typically glargine, which is associated with a higher hypoglycemic risk than degludec. This study will assess the efficacy and safety of Continuous Subcutaneous Insulin infusion (CSII) combined with Continuous Glucose Monitoring (CGM), as compared to Multiple Daily Injections (MDI) of insulin analogues, using degludec as basal insulin, associated with traditional self-monitoring of capillary blood glucose (SMBG) in patients with type 1 diabetes. A crossover design was chosen in order to minimize study sample improving statistical power.