Search Medical Condition
Please enter condition
Please choose location from dropdown

Cotignola, Italy Clinical Trials

A listing of Cotignola, Italy clinical trials actively recruiting patients volunteers.

RESULTS

Found (40) clinical trials

Micra Transcatheter Pacing System Post-Approval Registry

The Micra Registry is a global, prospective, observational, multi-site registry. Patients enrolled in the Micra Registry will be prospectively followed for a minimum of 9 years post-implant or until registry closure, patient death, patient exit from the registry (i.e., withdrawal of consent), or unless patient is participating in an acute ...

Phase N/A

0.0 miles

Learn More »

Epidermoid Cancer Development in Esophageal Achalasia

In order to define incidence and risk factors for epidermoid carcinoma 681 patients affected by esophageal achalasia observed since 1973 were followed up with no time limits according to a prospective follow-up protocol. The local institutional review board approved using the database from the division of thoracic surgery for research ...

Phase N/A

0.0 miles

Learn More »

GIse Registry Of Transcatheter Treatment of Mitral Valve regurgitaTiOn (GIOTTO)

The main objective is to achieve demographic and outcome data and identify predictors of clinical success, according to real-world Italian data. In addition the registry is designed to obtain health economic data to support reimbursement strategies in Italy. The study is focusing on MITRACLIP therapy since this is the leading ...

Phase N/A

0.0 miles

Learn More »

Laboratory Cellular and Molecular Determinants of Clinical Success in Diabetic Patients With Critical Limb Ischemia

All consecutive patients admitted to Maria Cecilia Hospital will be enrolled in the ECAD-CLI study. According to interventional management of the patient the following data and samples will be prospectively collected and related to outcome: medical history, cardiovascular risk factors, clinical presentation information related to angiography of peripheral arteries. An ...

Phase N/A

0.0 miles

Learn More »

Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products

All Medtronic market-released leads and all market-released IPG, ICD and CRT devices are eligible to be included in this study.

Phase N/A

0.0 miles

Learn More »

Product Surveillance Registry

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge ...

Phase N/A

0.0 miles

Learn More »

Frailty in Elderly Patients Receiving Surgical or Percutaneous Procedures for Valvular Disorders

This is a prospective study. This a single centre study involving the Maria Cecilia Hospital (Ravenna, Italy). The study is expected to enroll at least 450 consecutive patients with 70 years, which are admitted for: GROUP A: severe aortic stenosis undergoing surgical aortic valve replacement GROUP B: severe aortic stenosis ...

Phase N/A

0.0 miles

Learn More »

Scaffold in Emilia Romagna and in the MAGIC Network

Coronary stents are the default devices for the treatment of coronary artery disease in percutaneous coronary intervention (PCI) according to existing guidelines. However, thrombosis and restenosis are still the main limitations of current permanent metallic stents. In contrast to Bare Metal Stents (BMSs), Drug Eluting Stents (DESs) have a reduced ...

Phase N/A

0.0 miles

Learn More »

Minimally Invasive Versus Conventional Aortic Valve Replacement: a Long Term Registry

The study will focus on data recorded and collected from daily clinical treatment of patients undergoing isolated aortic valve replacement due to symptomatic aortic stenosis who consented to the use of their personal data. After surgery patients will be followed up to a minimum of 12 months. In-hospital and follow-up ...

Phase N/A

0.0 miles

Learn More »

IN.PACT BTK Randomized Study to Assess Safety and Efficacy of IN.PACT 014 vs. PTA

To assess the safety and efficacy of the paclitaxel drug-eluting balloon IN.PACT 014 versus conventional percutaneous transluminal angioplasty (PTA) for the treatment of patients with chronic total occlusions in the infrapopliteal arteries.

Phase N/A

0.57 miles

Learn More »