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NCT ID: NCT02630433 Completed - Pancreatitis Clinical Trials

Trial of Index Cholecystectomy Versus Scheduled Cholecystectomy in Biliary Pancreatitis

Start date: August 2009
Phase: N/A
Study type: Interventional

There are controversies optimal timing for cholecystectomy in patients with mild biliary pancreatitis. The safety of cholecystectomy performed during an episode of pancreatitis has been questioned. The aim of the present randomized controlled trial is to compare the outcome in terms of recurrent pancreatitis and gallstone-related events between index cholecystectomy, performed during the first admission for acute pancreatitis, and scheduled cholecystectomy, performed 4-6 weeks after discharge.

NCT ID: NCT02629406 Completed - Clinical trials for Diabetes Mellitus, Type 1

Studies on the Adaptive Responses to Hypoxia

HYKRAND
Start date: November 2015
Phase: N/A
Study type: Observational

The general aim of this study is to define the response to hypoxic challenge in patients with diabetes. The investigation will provide response for different questions that are central for explaining the development of complications in diabetes - have patients with diabetes an impaired reaction to adapt to hypoxia - what consequence has hypoxia challenge on respiratory and on cardiovascular regulation in patients with diabetes - what consequence has diabetes on the angiogenetic response to hypoxia

NCT ID: NCT02627885 Completed - Parkinson Disease Clinical Trials

Internet-CBT for Parkinsons Disease

Patrik
Start date: December 2015
Phase: N/A
Study type: Interventional

The aim of the study is to investigate if an Internet-based psychological treatment based on principles from Cognitive Behavioral Therapy can increase function and quality of life for patients with Parkinson disease.

NCT ID: NCT02627872 Active, not recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Clinical & Systems Medicine Investigations of Smoking-related Chronic Obstructive Pulmonary Disease

COSMIC
Start date: March 2007
Phase:
Study type: Observational

Chronic Obstructive Pulmonary Disease (COPD) is an increasing global health problem, which primarily increases among the female population. The purpose of this study is to perform in-depth clinical and molecular characterizations of early stage COPD patients, as well as healthy never-smoker and at-risk smoking control populations to identify molecularly related subgroups patients, including gender-related sub-phenotypes of COPD.

NCT ID: NCT02626546 Completed - Clinical trials for Postoperative Complications

Predictors, Risk Factors and Outcome Following Major Surgery

PROFS
Start date: November 2015
Phase:
Study type: Observational

This is a multicentre, prospective, observational cohort study. Consecutive patients, operated in six University Hospitals in Sweden will be recruited following major surgical procedure. The length of patient recruitment period will be 12 weeks. The length of follow up will be 360 days . The objectives are to determine the postoperative morbidity (during the hospital stay), the survival (0-360 days), to identify risk factors for adverse outcomes and to identify risk factors that may potentially be influenced by any intervention in the future. Amendments: 1. The follow-up of mortality is extended to 3 years of the cohort 2. The mortality of the background population at 30 and 90 Days will be analyzed 3. Validation of the Surgical Outcome Risk Tool in the study cohort and in the background population are planned

NCT ID: NCT02625896 Completed - Pain Clinical Trials

Free Fall Acrobatics to Reduce Neck Loads During Parachute Opening Shock: Evaluation of an Intervention.

ACROPOSE
Start date: June 17, 2017
Phase: N/A
Study type: Interventional

This study aims to evaluate the use of an aerial human body manoeuvre to reduce the biomechanical load on the neck of a parachutist during the parachute opening, in order to create a basis for future prevention of skydiver neck pain in the parachutist population.

NCT ID: NCT02625480 Active, not recruiting - Clinical trials for Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia

Study Evaluating Brexucabtagene Autoleucel (KTE-X19) in Pediatric and Adolescent Participants With Relapsed/Refractory B-precursor Acute Lymphoblastic Leukemia or Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma

ZUMA-4
Start date: February 1, 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objectives of this study are to evaluate the safety and efficacy of brexucabtagene autoleucel (KTE-X19) in pediatric and adolescent participants with relapsed/refractory (r/r) B-precursor acute lymphoblastic leukemia (ALL) or relapsed or refractory (r/r) B-cell non-Hodgkin lymphoma (NHL). As of October 2022, no further patients with acute B-cell Acute Lymphoblastic Leukemia (ALL) will be asked to join the study. The study remains open for recruitment for patients that have B-cell Non Hodgkin Lymphoma (NHL).

NCT ID: NCT02623608 Completed - Metabolic Syndrome Clinical Trials

Effects of Functional Ingredients in an Acute Metabolic Challenge Context

Start date: August 2015
Phase: N/A
Study type: Interventional

After an energy-rich meal the blood levels of glucose and lipids undergo a marked temporary increase, triggering a wave of oxidative stress due to the appearance of excess free radicals in adipose and muscle tissues. Elevated postprandial hypertriglyceridemia has been associated with increased risk of cardiovascular disease and type 2 diabetes. Hence, postprandial changes in different circulating biomarkers are potential predictors of cardiometabolic risk. In addition to the possibility of evaluating acute variations in metabolic risk markers in response to different types of fat, the metabolic challenge approach may serve as a challenge-meal background in order to reveal possible beneficial effects of specific food ingredients. In this study, circulating cardiometabolic disease-related biomarkers, including endotoxemia, will be assessed postprandially in search for beneficial actions of particular functional food ingredients consumed in combination with a high-fat meal.

NCT ID: NCT02622555 Completed - Overactive Bladder Clinical Trials

Cardiovascular Morbidity During Treatment of Overactive Bladder With B3 Agonists

Start date: August 2013
Phase: Phase 4
Study type: Observational

Overactive bladder syndrome complicates life for many women. 60-70% of women report improvement with treatment but the antikolinergic treatment is often limited by the adverse events, for example dry mouth, obstipation and urinary retention. Mirabegron is a b3-adrenoreceptor agonist which induces detrusor relaxation. Earlier studies has demonstrated similar efficacy comparing Mirabegron with antimuscarinics but a significant reduction of adverse events. The aim of the present study is to survey cardiovascular adverse events with Mirabegron treatment in a general population suffering from overactive bladder syndrome.

NCT ID: NCT02622490 Active, not recruiting - Metabolic Rate Clinical Trials

Acute Effects of Different Macronutrient Compositions and Meal Distributions of the Food

DIT2
Start date: September 2015
Phase: N/A
Study type: Interventional

About thirty participants, of varying degrees of obesity or being non-obese, without serious concomitant diseases consume either a high- or a low- carbohydrate beverage. The beverage is also consumed either as one single drink or as 5 small portions in the morning and are tested for effects on major cardiovascular risk markers and on metabolic rate for three hours on each occasion.