Flanders medical research program

Study with us: Projects for Masters and PhD candidates. Flinders University is recognised for making a difference locally and globally in rural and remote health. We have a considerable presence in rural and remote communities throughout South Australia and the Northern Territory. Northern Territory : the College has an extensive presence across the NT, and in true Top End style, our activities are well spread out: there are staff across our five locations in Darwin, Alice Springs, Katherine, Nhulunbuy and Tennant Creek.

South Australia : Flinders University Rural Health SA facilitates high quality multidisciplinary health education and research across rural communities in South Australia. Our campuses are located in Mt.

Gambier, Victor Harbor, Murray Bridge, the Barossa and Renmark, but we do also accommodate medical, nursing and allied health students on placement in some of the more remote regions of South Australia, including Coober Pedy, Roxby Downs and Ceduna.

Professor Peter Eastwood , Director. Dr Rebecca Keough , Institute Manager. Warning You have reached the maximum number of saved studies Listing a study does not mean it has been evaluated by the U. Federal Government. Read our disclaimer for details. Last Update Posted : August 1, Study Description. The objective of this study is to evaluate the safety and efficacy of recanalization of acute and subacute femoropopliteal stent occlusions with the Rotarex S catheter Straub Medical.

Detailed Description:. Arms and Interventions. Outcome Measures. Embolization, amputation, perforation or hemorrhage. Defined as a repeat intervention to maintain or re-establish patency within the region of the treated arterial vessel plus 5 mm proximal and distal to the treated lesion edge.

Defined as an improvement of Rutherford classification at 6 month follow-up of one class or more as compared to the pre-procedure Rutherford classification. Defined as any clinical event that is fatal, life-threatening, or judged to be severe by the investigator; resulted in persistent or significant disability; necessitated surgical or percutaneous intervention; or required prolonged hospitalization. Eligibility Criteria. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision.

Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials. More Information. National Library of Medicine U. Arms and Interventions. Outcome Measures. Primary Outcome Measures : primary patency [ Time Frame: 12 months post-procedure ] primary patency at 12 months, defined as a target lesion without a hemodynamically significant stenosis on duplex ultrasound systolic velocity ratio no greater than 2. Patients that present without a hemodynamically significant stenosis at the target area on duplex ultrasound systolic velocity ratio no greater than 2.

Clinical success at follow-up is defined as an improvement of Rutherford classification at 6-, month follow-up of one class or more as compared to the pre-procedure Rutherford classification.

Determined according the following classification on x-ray: Class 0 no strut factures ; Class I single tine fracture ; Class II multiple tine factures ; Class III Stent fracture s with preserved alignment of the components ; Class IV Stent fracture s with mal-alignment of the components ; Class V Stent fracture s in a trans-axial spiral configuration.

Defined as any clinical event that is fatal, life-threatening, or judged to be severe by the investigator; resulted in persistent or significant disability; necessitated surgical or percutaneous intervention; or required prolonged hospitalization.

Eligibility Criteria. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.

More Information. National Library of Medicine U.