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Internal Medicine clinical trials

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NCT ID: NCT05756400 Active, not recruiting - Internal Medicine Clinical Trials

Polypharmacy Among Internal Medicine Patients

Start date: January 1, 2023
Phase:
Study type: Observational

The World Health Organisation Patient Safety Challenge: Medication Without Harm has brought our attention to the importance of medication-related harm as a global public health issue. One of the major contributing factors is polypharmacy, the usage of multiple medicines at the same time. People are getting older and living longer with chronic diseases; they need more medications, which frequently leads to polypharmacy. Subsequently, they are at more risk of medication-related harm. The planned project is an epidemiological study on polypharmacy, medication appropriateness, risk factors, and clinical outcomes post-discharge from a hospital for internal medicine patients. The study group hypothesise that pre- and post-admission polypharmacy and potentially inappropriate prescribing is common, especially among older patients, patients with a high comorbidity and frailty burden. Our hypothesis is additionally that preadmission polypharmacy and potentially inappropriate prescribing is associated with higher short- and long-term mortality, a longer primary hospitalization length of stay, and a higher risk of readmission.

NCT ID: NCT05546034 Completed - Internal Medicine Clinical Trials

Nutrition Screening - Route to a More Practical Method

Start date: September 6, 2021
Phase:
Study type: Observational

Observational study. Comparison of existing nutritional screening tools based on questionnaires with blood tests already performed on a routine basis. No intervention undertaken.

NCT ID: NCT04797130 Completed - Pulmonary Disease Clinical Trials

The Effect of Hospital Fit 2.0 on Patients Physical Activity

Start date: March 23, 2021
Phase: N/A
Study type: Interventional

The primary objective of this study is to investigate if using Hospital Fit 2.0 as part of the usual care physiotherapy treatment of patients hospitalised at the department of Internal Medicine and the department of Pulmonology in MUMC+ will result in an increase in the amount of PA performed compared to patients who do not use Hospital Fit 2.0 as part of the physiotherapy treatment.

NCT ID: NCT04139265 Completed - Iron-deficiency Clinical Trials

Transferrin Saturation Coefficient and Ferritinemia in Diagnosis of Iron Deficiency

CarenceMartial
Start date: June 6, 2019
Phase:
Study type: Observational

Transferrin saturation coefficient and ferritinemia in diagnosis of iron deficiency

NCT ID: NCT03188211 Completed - Atrial Fibrillation Clinical Trials

E-learning to Improve Oral Anticoagulant Use in Hospitalized Older People With AF

SIM-AF
Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Atrial Fibrillation (AF) is the most common cardiac arrhythmia and the main cause of cardioembolic stroke. Oral Anticoagulation (OAC) has been shown to significantly prevent AF-related thromboembolism, however, despite convincing evidences and current guidelines recommendations, OAC tends to be underused in clinical practice especially in the oldest. Education and training to appropriately select people suitable for OAC for stroke prevention could be pivotal in the decision making process. According to the study project, physicians working in Internal Medicine and Geriatric wards, where are mainly admitted elderly people with AF, will undergo to a program of e-learning through computer-based simulation method reproducing clinical scenarios of patients aged 65 years or older, with known or newly diagnosed AF, admitted to hospital for any medical reason and requesting that a decision about long-term antithrombotic therapy is taken. Primary objective of the study is to investigate whether such educational intervention will improve the appropriate use and prescription rate of OAC in hospitalised elderly patients with AF, multimorbidity and polypharmacy, in comparison to the usual practice. The study will be a cluster randomised controlled trial involving a network of Internal Medicine and Geriatrics wards. Thirty-two wards will be recruited based on voluntary participation and randomised to receive an educational intervention through computer-based simulation, (N=16) or to continue with the usual practice (N=16). Subjects receiving the intervention will be all the staff physicians of the wards randomised in the intervention arm. The impact of the intervention compared with the usual practice will be evaluated in patients aged 65 years or older admitted to the participating centres with a known diagnosis of AF or newly diagnosed with AF during the hospitalisation.

NCT ID: NCT01418846 Completed - Pediatrics Clinical Trials

Determination of Voriconazole Levels in Saliva - Validation in Specific Subsets of Patients

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

The purpose of this study is to investigate the intra-saliva penetration of voriconazole in different subpopulations. The goal is to develop, optimize and validate an easy, non-invasive and painless procedure for Therapeutic Drud Monitoring of voriconazole that can be used in children, ambulatory patients and in patients in whom blood drawing is difficult.