Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

the Role of cArdiac Inflammation, endoThelial Dysfunction, and FIbrosis in fabrY Disease

The overall objective of this study is to investigate Fabry-related cardiomyopathy and the use of native T1-mapping, coronary microvascular function, cardiac inflammation, and cardiac injury in an effort to improve the ability to detect disease. The study aims to achieve this by: 1. Investigating the association between cardiac inflammation, fibrosis, and injury against the distribution and degree of microvascular disease in patients with Fabry disease with and without left ventricular hypertrophy (LVH) using cardiac magnetic resonance (CMR) imaging and 82Rubidium Positron emission tomography and computer tomography (82Rb-PET/CT). 2. Using an extensive, in-depth biomarker blood panel to investigate the pathological pathways associated with Fabry disease and Fabry-related cardiomyopathy.

Participants needed: 54
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Caroline Michaela KistorpUpdated: Apr 8, 2025Locations: 1
Eligibility criteria

Male and female individuals with a genetically-verified diagnosis of Fabry disea... [+2]

Any contraindication against a pharmacologically induced rest-stress PET/CT prot... [+13]

Status: Recruiting

Fibrosis, Inflammation, Oxygenation of Renal Tissue In FabrY Disease

The overall objective of this study is to investigate Fabry-associated renal organ involvement by using a novel magnetic resonance imaging (MRI) approach, focusing on changes in renal oxygen levels by blood oxygenation-level dependent (BOLD) imaging. Furthermore, to correlate renal oxygenation to the phenotypic presentation of patients with Fabry-associated nephropathy regarding circulating and imaging-derived biomarkers of kidney inflammation, fibrosis and injury as compared with healthy age- and sex-matched controls. The study will achieve this by: 1\) Using a non-invasive, contrast-free MRI protocol focusing on parameters of oxygenation, inflammation, fibrosis, and injury in the kidney. 2\) Using an extensive, in-depth biomarker blood panel to investigate the pathological pathways associated with Fabry disease and Fabry-associated nephropathy.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Caroline Michaela KistorpUpdated: Apr 6, 2025Locations: 1
Eligibility criteria

Male and female individuals (≥18 years of age) [+1]

Any contraindication for magnetic resonance imaging according to standard checkl... [+11]

Status: Recruiting

Prospective, Longitudinal Study on FItness DOping in DenmarK

The aim of this prospective longitudinal study is to investigate the risks associated with use of anabolic steroids in fitness circles in Denmark in order to assess the scope of therapeutic need existing as a consequence of use. The objectives are: * To assess long-term complications and outcomes related to: cardiovascular disease, diabetes, gonadal disease (women and men) and psychiatric disease using data from Danish registries including addressing central questions such as whether the following characteristics play a role for development of overt disease * Characterization of illicit AAS use among men and women * Current male reproductive health * Current psychological well-being, aggressive tendencies, cognitive function and quality of life * Current cardiovascular and metabolic status The participants will undergo: * Semi-structured medical interview * Physical examinations * Questionnaires * Blood and urine sampling * Dual X-ray Absorptiometry With a subset undergoing further testing, including semen analysis, gonadotropin-releasing hormone (GnRH) and human chorionic gonadotropinm (hCG) stimulation and 82Rubidium positron emission tomography and computer tomography (PET/CT). Register-based follow-up is planned every third year until the 15th year, marking the completion of the trial. The study will include 800 participants with current or former AAS use and 100 participants (80 male; 20 female) as controls with no former or current use of AAS.

Participants needed: 900
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Caroline Michaela KistorpUpdated: Feb 15, 2024Locations: 1Duration: 15 Years
Eligibility criteria

Severe psychiatric or somatic diseases which makes it impossible to give informe... [+1]