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Objectives |
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The primary objective of TED electronic-based registry is to evaluate the outcome of Paclitaxel eluting Taxus Element stent in 750 Patients with diabetes mellitus who are suitable for drug-eluting stent implantation according to the applicable |
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guidelines on percutaneous coronary interventions. .....Read more |
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Overview |
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T.E.D "Taxus Element in Diabetics Registry"
is a prospective multi-country, multi-center, observational, open-label medical registry designed to electronically capture data, manage, monitor, and report in diabetic patients' outcomes receiving Paclitaxel eluting Taxus Element Stent. |
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TED is designed to be non experimental study, where all enrolled patients should be treated according to the current routine hospital practice and standards of care.
TED patient population are only those patients with diabetes mellitus suitable for drug-eluting stent implantation according to the applicable guidelines on percutaneous coronary interventions. |
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Project Description |
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Diabetes has always adversely affected the outcome of percutaneous coronary intervention (PCI) first angioplasty and then later stenting. Patients with diabetes mellitus are known to have a higher adverse event rate after PCI and stenting compared with those without diabetes. This is mainly due to increased restenosis and subsequent need for repeat revascularization. |
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Patients with diabetes have often .......Read more |
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TED Medical Centers |
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Saudi Arabia |
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United Arab
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Lebanon |
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Tunisia |
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Iran |
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Pakistan |
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TED Login |
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TED Study Stent |
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"The C.E. marked Paclitaxel eluting Taxus Element stent of (Boston Scientific, Natick, Massachusetts)" |
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Participated Countries |
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Five countries from across the Middle-east, North Africa and Asia are participating in TED study : - Saudi Arabia - United Arab Emirates - Lebanon - Tunisia - Iran - Pakistan |
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Ethical Considerations |
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An ethics approval letter will be obtained from the ethics committee of each individual participated hospital.
Despite the fact that TED study is not altering the standard treatment and any related medical procedures, A consent form is to be collected from each individual patient enrolled in the study.
Names and identities for all individuals are un-identified during the study and all submitted data will remain encrypted from data entry to data analysis & study publications.
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