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Blankenberge, Belgium Clinical Trials

A listing of Blankenberge, Belgium clinical trials actively recruiting patients volunteers.

RESULTS

Found (30) clinical trials

The Treatment of Clavicular Fractures

Patients with a displaced, shortened, midshaft clavicular fracture are randomized in two groups: conservative or operative treatment. The conservative arm is treated with a sling for 6 weeks. The operative arm is treated with osteosynthesis, within 2 weeks. Patients are clinically and radiologically evaluated during 1 year. A economical analysis ...

Phase N/A

6.45 miles

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Tysabri Observational Program

TOP is an epidemiological observational study of participants receiving natalizumab, with each participant to be followed for up to 15 years. This study is designed to address the long-term safety profile and the long-term impact on disease activity and progression of Tysabri with marketed use, and the impact of treatment ...

Phase N/A

6.45 miles

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International Collaborative Gaucher Group (ICGG) Gaucher Registry

The ICGG Gaucher Registry is an ongoing, international multi-center, strictly observational program that tracks the routine clinical outcomes for patients with Gaucher disease, irrespective of treatment status. No experimental intervention is involved; patients in the Registry undergo clinical assessments and receive care as determined by the patient's treating physician. The ...

Phase N/A

6.45 miles

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Study Comparing Legflow Versus Bare Balloon Angioplasty for Treatment of Atherosclerotic Disease

This interventional study will collect data about the treatment of de novo lesions or restenotic lesions. Restenotic lesions that are previously DCB (drug coated balloon) treated or in-stent restenosis are excluded in this study. The primary objective of this randomized study is to compare the efficacy of the DCB (Legflow ...

Phase N/A

6.45 miles

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Comparison of VT Ablation Outcomes Using Remote MAGNETIC Navigation Versus Manual Approach in a Low LVEF Population

This study is a randomized, single-blind, prospective, multi-center post market evaluation. Subjects will be screened for study eligibility and asked to complete written informed consent prior to any study specific testing assessments. After completing written informed consent, a total of 386 subjects will be randomized on a 1:1 basis to ...

Phase N/A

6.45 miles

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Serratus Intercostal Plane Block in Video Assisted Thoracic Surgery

The proposed randomized controlled trial aims at comparing the opioid use per- and postoperatively in patients with versus without SIP block undergoing VATS. We hypothesize that use of a SIP block results in less opioid use during and the first 24 hours after VATS as compared with patients without SIP ...

Phase N/A

6.45 miles

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Invasive Pulmonary Aspergillosis Complicating Influenza Infection

This prospective multicentre case-control registration study in Dutch and Belgian ICUs will assess the difference in incidence and outcome of invasive pulmonary aspergillosis (IPA) in ICU patients with severe influenza compared with influenza-negative control patients with severe community-acquired pneumonia during the coming three influenza seasons (2017-2020). The study will further ...

Phase N/A

6.45 miles

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Pulmonary Vein Isolation With Versus Without Continued Antiarrhythmic Drugs in Persistent Atrial Fibrillation

Background: In real-life, ADT is often continued after catheter ablation for persistent AF. No study investigated whether ADT continued beyond the blanking period reduces recurrence after a first ablation for persistent AF. Purpose: The aim of this trial is to investigate whether continued ADT (ADT ON) reduces recurrence of atrial ...

Phase N/A

6.45 miles

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Catheter Ablation of All Inducible AT Post AF Ablation

In the treatment of symptomatic drug resistant persistent atrial fibrillation (Ps AF), catheter ablation has a class IIA indication. During the follow-up, a significant amount of patients (~50%) will experience atrial tachycardias (AT) recurrence. The endpoint of AT ablation during the second procedure has not been validated. At present, several ...

Phase N/A

6.45 miles

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Anesthesia Followup of All Bariatric Procedures at One Hospital

Every patient undergoing a bariatric procedure is entered in the data base after the procedure is finished, based on the information available in the medical records. the study has no end point and keeps collecting data as long as procedures are performed. The data is analyzed intermittent when medical questions ...

Phase N/A

6.45 miles

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