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NCT ID: NCT05515159 Enrolling by invitation - Depression Clinical Trials

Blood Biomarkers in Electroconvulsive Therapy

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

The present multi-disciplinary study will assess blood biomarkers to investigate putative mechanisms of action of ECT. Laboratory findings will be correlated to clinical parameters, cognitive measures and psychometric outcome measures. The aim is to elucidate the underlying mechanisms for both treatment effects and cognitive side effects of ECT.

NCT ID: NCT05400278 Enrolling by invitation - Clinical trials for Bardet-Biedl Syndrome

Characterizing the Genotype and Phenotype in Adults With Bardet-Biedl Syndrome

Start date: February 1, 2022
Phase:
Study type: Observational

Bardet-Biedl syndrome (BBS; OMIN #209900) is a rare genetic disorder characterized by six core features: rod-cone dystrophy (retinitis pigmentosa), polydactyly, obesity, genital anomalies, renal anomalies, and learning difficulties. This study aims to contribute to genetic and medical knowledge of BBS, and to provide information on quality of life in adults with BBS and their close relatives. Participants will undergo medical assessments (ocular, oral, and physical examinations) and self-reporting of quality of life, diet, cognitive and emotional symptoms. There are some known genotype-phenotype associations in BBS and participants will be offered genetic testing. It is important to map both genotype and associated phenotype in order to provide optimal treatment and follow-up. Individuals with BBS, age 16 years or older, will be invited to participate. The investigators expect to enroll at least 25 male and female adults with BBS and 15 of their parents to participate in qualitative interviews. These interviews will investigate parents' experiences having a child with BBS, satisfaction with health care services, experience with social and family life, and psychological health.

NCT ID: NCT05207917 Enrolling by invitation - Obesity Clinical Trials

How Does Bariatric Surgery Affect Social Experiences and Well-being - The BaSES-study

BaSES
Start date: May 12, 2022
Phase: N/A
Study type: Interventional

Nonrandomized controlled trial to assess whether or not sleeve gastrectomy (SG) and Roux-en-Y gastric bypass (RYGB) affect social experiences and biomarkers of well-being differently 6 weeks and 1 year after surgery. The decision whether SG or RYGB will be performed is determined by medical decision making. Hypotheses Bariatric surgery influences social experiences and well-being through changes in body image, reward responsivity and gut hormones . These changes may differ between gastric bypass (RYGB) and sleeve gastrectomy (SG).

NCT ID: NCT05119387 Enrolling by invitation - Clinical trials for Amyotrophic Lateral Sclerosis

Genetic Study of Amyotrophic Lateral Sclerosis in Norway

GAIN
Start date: August 1, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to explore the genetic causes relevant for ALS development in Norway.

NCT ID: NCT05117606 Enrolling by invitation - Clinical trials for Monitoring, Physiologic

LYNG21: Ably LYNG Clinical Demonstration in Operative Environment

LYNG21
Start date: May 25, 2021
Phase: N/A
Study type: Interventional

The study main objective will be to compare measurements of heart rate, respiration rate, blood pressure and movement done by LYNG by Ably Medical with the corresponding measurements made by standard equipment in a patient sample in a hospital setting. The comparison will show the degree of agreement between LYNG and the existing current standard equipment. Data from the study will support Ably Medical in optimizing the LYNG product and measurement precision.

NCT ID: NCT05057338 Enrolling by invitation - Multiple Sclerosis Clinical Trials

Functions, Physical Activity and Employment for Individuals With MS: A Pilot Feasibility Study

CoreDISTp
Start date: August 27, 2021
Phase: N/A
Study type: Interventional

Multiple Sclerosis (MS) is a chronic disease affecting young adults. Impaired balance, walking, reduced physical activity and participation in employment are common, however, less integrated in the health care. The researchers have developed a multidisciplinary intervention and pathway delivered across health care levels targeting the promotion of balance, walking, physical activity and participation in employment. The research team will perform a pilot feasibility Randomized Controlled Trial (RCT) and interviews to investigate the feasibility of the new intervention compared to a standard care for individuals with lower levels of disability.

NCT ID: NCT05039229 Enrolling by invitation - Hypersensitivity Clinical Trials

Measures for Bioaerosol Reduction in the Salmon Industry

SHInE
Start date: September 20, 2021
Phase: N/A
Study type: Interventional

Workers in the salmon industry are at risk of developing allergies and respiratory diseases, including asthma, due to occupational exposure to bioaerosols, i.e. biological agents such as allergens, enzymes and endotoxins, in their work environment. The overall objective of this intervention trial is to identify effective and feasible control measures (interventions) that reduce exposure to these bioaerosols. The project comprises nine salmon processing factories in northern, central and western Norway. The factories are allocated to either one of the two intervention arms or the control group. In all factories, an assessment of exposure to bioaerosols will be performed. In addition, employees will be invited to undergo a health examination and fill out a self-administered questionnaire including information on demographics, work tasks, health and health promoting factors. The intervention trial is part of a broader study that comprises several substudies including the identification of clinically relevant allergens, investigation of exposure-response relationship between the exposure to individual bioactive agents in bioaerosols and investigations of prevalence of airway symptoms, altered lung function, skin symptoms or immunological responses indicating hypersensitivity. Finally the project includes the identification of health promoting factors that are present in the salmon processing industry. The project is an interdisciplinary multi-center study that places great emphasis on a close dialogue between the researchers and industry in all phases of the project.

NCT ID: NCT04957719 Enrolling by invitation - Clinical trials for Acute Myocardial Infarction

Selatogrel Outcome Study in Suspected Acute Myocardial Infarction

SOS-AMI
Start date: August 14, 2021
Phase: Phase 3
Study type: Interventional

This study will randomize patients recently discharged from the hospital with a confirmed diagnosis of type 1 acute myocardial infarction (Thygesen et al. 2018) and having additional cardiovascular risk factors.

NCT ID: NCT04886934 Enrolling by invitation - Cardiac Disease Clinical Trials

Temporary Epicardial Pace Wire With Integrated Sensor for Continuous Postoperative Monitoring of Myocardial Function

Start date: October 25, 2021
Phase: N/A
Study type: Interventional

Transesophageal echocardiography is used to monitor cardiac wall motion at various time points during open-heart surgery. After surgery, the measurements are made at various time points by transthoracic echocardiography. The CS1 system enables continuous, direct measurement of cardiac wall motion. This is achieved through use of temporary pacemaker wires incorporating a motion detector called an accelerometer. Use of TMEs during and after open-heart surgery is part of the normal clinical routine. Continuous monitoring of cardiac wall motion during and after surgery can quickly highlight the need for medical intervention with cardiac drugs and allow very early detection of potentially serious complications leading to abnormal cardiac wall motion. Cardiac wall motion activity registered by the CS1 system and echocardiography at specific time points during and after surgery will be analyzed to see how well they compare.

NCT ID: NCT04841044 Enrolling by invitation - Healthy Diet Clinical Trials

Health Effects of Cetoleic Acid (A Randomized Double Blinded Controlled Trial)

Start date: April 27, 2021
Phase: N/A
Study type: Interventional

In this Randomized Controlled Trial (RCT) we want to study how supplements of cetoleic acid ( C22:n1-11) (intervention) affect the conversion of alpha-linolenic acid (ALA) to EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid) in healthy subjects, compared to supplements with a low concentration of cetoleic acid (control). Our primary endpoints are changes in the concentration of EPA and DHA in plasma and red blood cells.