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NCT ID: NCT02650531 Completed - Stroke Clinical Trials

Norwegian COgnitive Impairment After STroke (NorCOAST) Study

Nor-Coast
Start date: May 2015
Phase:
Study type: Observational

A prospective observational multicenter study aiming to describe incidence, and identify predictors for development of poststroke dementia (PSD) and mild cognitive impairment (MCI) after stroke

NCT ID: NCT02649296 Recruiting - Arthrosis Clinical Trials

Effect of Skanlab Regarding Knee Arthrosis

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

The purpose is to find out the effect of Skanlab at knee arthrosis.

NCT ID: NCT02649114 Completed - Clinical trials for Stress Disorders, Post-traumatic

Eating Disorders With and Without Childhood Trauma

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

The combination of EDs (ED) and post-traumatic sequelae of childhood trauma leads to significant impairment, suffering and represents a public health concern because it is frequently associated with role impairment, and is frequently under-treated. Considering the severity of these conditions, there is a need to develop more effective treatments that are tailored to the specific needs of these patients as no conclusion has been made about the treatment of choice. To improve treatment it is critically important to study treatment effects and the mechanism of these effects.

NCT ID: NCT02648165 Completed - Major Depression Clinical Trials

Secondary Prevention of Depression Through Group-based ACT-Therapy Preceded by an Experimental ABM-Procedure

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

Depression (major depressive disorder; MDD) is a very common mental disorder. Research suggests that individuals with prior depressive episodes have a risk of the relapse or recurrence of MDD. Secondary prevention has been identified as a key goal in the long-term management of the disease. The current project aims to investigate whether group based Acceptance and Commitment Therapy (ACT) can reduce surrogate and clinical markers of relapse in a group highly vulnerable to depressive episodes. The group intervention will consist of eight sessions, and each group will consist of maximum 12 persons. The project also studies whether Attention Bias Modification (ABM) preceding the ACT intervention will enhance the effect. ABM will be administered over a fourteen days period prior to the ACT-intervention. Effect will be measured over a period of 12 months. The primary outcome is changes in depressive symptoms. ACT-specific secondary outcome measures are also included. Subjects with a history of major depression (n=200), currently in remission, will be recruited from Sørlandet Hospital (100 participants). Matched participants (100 participants) will be recruited at the University of Oslo. In the first phase, participants from Sørlandet hospital will be randomized to ABM treatment or control condition. In the second phase all participants from Sørlandet hospital will receive group based ACT treatment. Group based ACT and ABM represent interventions that are time and cost effective, and that could be made available to large number of individuals struggling with MDD.

NCT ID: NCT02648061 Completed - Clinical trials for Out-of-Hospital Cardiac Arrest

Transitions Between Clinical Circulatory States After Out-of-hospital Cardiac Arrest

Start date: January 2016
Phase:
Study type: Observational

Extensive research exists for cardio-pulmonary resuscitation (CPR) and the chance of successful return of spontaneous circulation (ROSC) is improved. Unfortunately, the overall prognosis after ROSC has not improved much and the in-hospital mortality is still reported to be 50 to 70 %. The "post-resuscitation disease" is now called the "post-cardiac arrest syndrome" (PCAS) and comprises 1) brain injury, 2) myocardial dysfunction and 3) systemic ischemia and reperfusion. Treatment of patients after cardiac arrest has often followed guidelines that were primarily developed for treatment of septic shock. It is still uncertain whether this is the optimal way to deliver circulatory support after cardiac arrest. There is a lack of studies assessing the relationship between the inflammatory response measured by inflammatory biomarkers and circulatory failure in PCAS. In this study a detailed description will be given of the clinical trajectory of the circulation and the inflammatory response during the first 5 days after cardiac arrest, and it will be investigated whether patterns of circulatory and inflammatory response may be predictive of deterioration of clinical state.

NCT ID: NCT02647970 Completed - Healthy Clinical Trials

Stearoyl-CoA Desaturase and Energy Metabolism in Humans

SEM
Start date: February 2016
Phase: N/A
Study type: Interventional

The aim of this study is to examine if changing stearoyl-coenzyme A desaturase-1 (SCD1) activity through dietary interventions can increase energy metabolism in humans.

NCT ID: NCT02647619 Completed - Clinical trials for Dupuytren Contracture

Dupuytren´s Disease Study. Primary Disease, MCP Joint, Xiapex, PNF

Start date: October 2013
Phase: Phase 4
Study type: Interventional

Aim: Clinical RCT comparing functional results and recurrence rate following enzymatic treatment vs. needle aponeurotomy. Materials and methods: 30° or more contracture of only one metacarpophalangeal (MCP) joint contracture of one of the three ulnar digits and less than 20° for the adjacent proximal interphalangeal (PIP) joint. Patients with primary disease of the hand. Total of 80 patients needed to detect difference of 13.5°. 1) Needle aponeurotomy 2) Clostridium Histolyticum treatment. Clinical follow ups 1,4 weeks, 16 weeks and 1,2 and 5 years. Functional outcome scores: URAM, Quick Dash, EQ5D, brief MHQ, VAS pain and VAS patient satisfaction. Total passive extension contracture reduction, recurrence rate and registration of complications.

NCT ID: NCT02647099 Active, not recruiting - Colorectal Cancer Clinical Trials

Adjuvant Low Dose Aspirin in Colorectal Cancer

ALASCCA
Start date: April 7, 2016
Phase: Phase 3
Study type: Interventional

ALASCCA is a randomized, parallel group, double blind, multicenter, placebo-controlled, biomarker-based study of adjuvant treatment with low dose aspirin in patients with colorectal cancer. Hypothesis is that patients diagnosed with colorectal cancer and somatic mutations in PI3K pathway can significantly improve survival if treated with low dose aspirin.

NCT ID: NCT02646553 Recruiting - Cushings Syndrome Clinical Trials

Saliva Cortisol Measurement as a Screening Test for Suspicious Cushings Syndrome in Children.

Start date: May 2012
Phase: N/A
Study type: Observational

Cortisol overproduction ( Cushings syndrome) is a condition where the patient have a special fat distribution, with accumulation of fat around the abdomen and in the neck, with thinner limbs and weak musculature. The condition can be difficult to separate from adipositas in general. Screening for hypercortisolism in adults has been easier the last years, because we can measure free cortisol in saliva samples at late night. In children we still dont have reference ranges for saliva cortisol in children, so the screening is still troublesome, based on Collection of 24-hour urine.The meaning of this study is to establish reference ranges for saliva cortisol, and evaluate in a cohort with adipose children if screening with saliva cortisol is sensitive and specific enough to be the New screening test for hypercortisolism in children too.

NCT ID: NCT02644564 Completed - Rotator Cuff Tear Clinical Trials

Early Clinical Examination and Ultrasonography Screening of Acute Soft Tissue Shoulder Injuries

Start date: October 5, 2015
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether the introduction of early ultrasonography screening will change the diagnostic spectrum of soft tissue shoulder injuries in patients aged forty years or more. We also want to study whether certain physical tests will be able to predict or rule out full-thickness tears of the rotator cuff (shoulder tendons) in the acute phase. Another purpose is to explore the course of soft tissue shoulder injuries over a year, as well as to compare the results to studies on the prevalence of rotator cuff full-thickness tears.