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Kraslavas Aprinkis, Latvia Clinical Trials

A listing of Kraslavas Aprinkis, Latvia clinical trials actively recruiting patients volunteers.

Found (60696) clinical trials

A Single Inhalation Dose Study to Assess Efficacy Pharmacokinetics (PK) Safety and Tolerability of AZD8871 in Patients With Long-term Lung Diseases.

This randomized, double-blind, placebo and active-controlled crossover study will be conducted at 5 sites in Germany and the United Kingdom (UK). Approximately 180 patients will be screened in order to randomize 72 patients into the study. Based on previous studies estimate, it is anticipated that 54 patients will be evaluable ...


Artificial Intelligence to Assess the Association Between Facial Characteristics and Coronary Artery Diseases

Several age-related appearance factors were described associated with increased risk of coronary artery diseases (CAD). However, several limitations made these facial risk factors hard to be utilized in clinical practice, including 1) low prevalence in CAD patients, 2) lack of specific definition, 3) poor reproducibility in artificial recognition. Thus, the ...

Phase N/A

Proton Craniospinal Irradiation With Bone Sparing to Decrease Growth Decrement From Radiation

This research study is a Pilot Study to determine whether using proton therapy in participants that require craniospinal radiation (whole brain and spinal cord radiation therapy) with sparing of the bony spine will work. This is the first time investigators are examining bone sparing proton therapy in pediatric craniospinal radiation. ...

Phase N/A

Combining tDCS With VR-based Motor Training in Stroke

Stroke represents one of the main causes of adult disability and will be one of the main contributors to the burden of disease in 2030. However, our healthcare systems do not have enough resources to cover the current demand let alone its future increase. There is a need to deploy ...

Phase N/A

Youth FORWARD Phase 1 YRI and EPP Study

Pilot study aims To examine the psychometric properties of an existing measures battery as well as a new battery for third-party reporting, To assess and adjust as needed structures for training and supervision, including the ICTA, and methods for conducting process evaluations of implementation procedures, and; To assess the feasibility ...

Phase N/A

Trial to Confirm the Clinical Efficacy and Safety of Dasiglucagon in the Treatment of Hypoglycemia in Subjects With T1DM

A randomized, double-blind, parallel-group trial to confirm the clinical efficacy and safety of dasiglucagon in the rescue treatment of hypoglycemia in subjects with type 1 diabetes mellitus (T1DM) compared to placebo


The Value of Placental Vascularization and Placental Volume in Pregnancy in APLS

APLS can be primary when no evidence of autoimmune disease is found, or secondary to autoimmune processes like systemic lupus erythematous (SLE) in a 40% of the cases.

Phase N/A

Group ("Project Life Force") vs. Individual Suicide Safety Planning RCT

Worldwide someone dies by suicide every 40 seconds. In the United States, Veterans exhibit significantly higher suicide risk when compared to the general United States population. One in five suicide deaths is a Veteran and in spite of enhanced suicide prevention services in the Veterans Administration (VA), twenty Veterans commit ...

Phase N/A

Neurorehabilitation After Traumatic Brain Injury: Functional Magnetic Resonance Imaging Study

Cognitive impairment following moderate to severe traumatic brain injury are usual. To date, cognitive rehabilitation effects on cerebral plasticity and quality of life remain unproven essentially because of methodological biases. Transcranial Direct Current Stimulation is an innovative technique of noninvasive brain stimulation that showed efficacy in literature. The current study ...

Phase N/A

Stress and Feeding (SAFE): A Pilot Intervention for Mothers and Their Preterm Infants

Descriptive statistics will be computed for demographic and outcome variables. The number of mother/infant dyads recruited but not enrolled will be tracked. If provided, reasons for non-participation will be noted. Enrolled dyads will be tracked and monitored for the number of times the interventions are used and completeness of study ...

Phase N/A