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Frederiksburg, Denmark Clinical Trials

A listing of Frederiksburg, Denmark clinical trials actively recruiting patients volunteers.

RESULTS

Found (696) clinical trials

Safety and Tolerability Study of AZD4831 in Patients With Heart Failure.

This is a randomized, double-blind, placebo controlled, parallel group, multicentre study in patients with Heart Failure with preserved Ejection Fraction (HFpEF) and mid-range Ejection Fraction (HRmrEF). The study will be conducted at approximately 10 sites in 5 countries (USA, Sweden, Denmark, Finland, Netherlands). Patients suitable for the study will be ...

Phase

0.0 miles

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Treatment of Knee Osteoarthritis With PAAG-OA

This is a multi-center, randomized, double-blind clinical investigation to compare the effectiveness of intra-articular polyacrylamide hydrogel (PAAG-OA) and a hyaluronic acid, Synvisc-One to induce symptomatic benefit in subjects with knee osteoarthritis.

Phase N/A

0.0 miles

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Comprehensive Treatment of Angina in Women With Microvascular Dysfunction

Coronary microvascular dysfunction is found to be associated with a significant adverse prognosis. The condition is strongly associated with increased future risk of major cardiovascular events, frequent hospital readmission, continued angina and loss of quality of life compared to the general population. Pathophysiology of microvessel disease: In the heart 95% ...

Phase N/A

0.38 miles

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Clinical Data Validation of Novel Wireless Cortrium C3 Monitor for Continuous Electrocardiogram Measurements

Development of new cost effective mobile devices and wireless technology has great potential in supervision of critically ill patients in wards as well as ambulant. Through continuous wireless monitoring in both the hospital and the patients home, detection of heart arrhythmias such as atrial fibrillation (AF) will be possible. AF ...

Phase N/A

0.38 miles

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Does Treatment With GLP-1 Reduce Alcohol Intake in Patients With Alcohol Dependence?

Number of patients and target population: 144 patients with a diagnosis of alcohol dependence and 25 healthy participants (described later). The patients included in the trial will be treated for 26 weeks with once-weekly subcutaneous injection of Bydureon (exenatide) 2 mg or placebo. The medication will be provided as a ...

Phase

0.38 miles

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The Danish Non-vitamin K Antagonist Oral Anticoagulation Study in Patients With Atrial Fibrillation

No randomized head-to-head comparison between the individual Non-vitamin K Antagonist Oral Anticoagulants (NOAC) exists, but such data are warranted to evaluate if the four NOACs are equal in stroke prevention without an additional cost of increased bleeding risk. Furthermore, classic randomized trials are highly selective, as elderly and/or fragile patients ...

Phase

0.38 miles

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The Danish Non-vitamin K Antagonist Oral Anticoagulation Study in Patients With Venous Thromboembolism (DANNOAC-VTE)

No randomized head-to-head comparison between the individual Non-vitamin K Antagonist Oral Anticoagulants (NOAC) exists, but such data are warranted to evaluate if the four NOACs are equal in treatment of venous thromboembolism (VTE) without an additional cost of increased bleeding risk. Furthermore, classic randomized trials are highly selective, as elderly ...

Phase

0.38 miles

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Effect of 12 Weeks of Acupuncture on AMH and COH in Low Responder Patients

AMH is measured cycle day 2 or 3 before and after 12 weeks of acupuncture and the levels are compared. Furthermore, secondary outcomes from IVF treatments before and after the intervention are compared.

Phase N/A

0.38 miles

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Outpatient PDD Guided Laser Mediated Destruction of Bladder Tumors

A prospective randomized two-part clinical trial comprising patients with recurrent pTa low grade bladder tumors. Study objectives and purpose: 1st Objective: To evaluate whether small pTa bladder tumours can be removed with diode laser in an outpatient department with similar efficacy as by TUR-BT resection in the operating theatre. 2nd ...

Phase N/A

0.38 miles

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Early Rheumatoid Arthritis COR Intervention

The study is a prospective randomised open, blinded endpoint trial with balanced randomisation (1:1) conducted in seven outpatient clinics in Denmark. Follow-up visits for patients in the intervention group are scheduled to occur at baseline and then after 2, 4 and 12 weeks and thereafter every third month for 5 ...

Phase N/A

0.38 miles

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