The Promus Element Rewards Study

Status unconfirmed

Conditions studied: Coronary Stenosis

In brief

This study is being done to study stent deformation on persons with de novo coronary lesions to determine how much deformation takes place and how often. The information gathered from the group that receives the Promus element stent will be compared to other groups that receive other contemporary drug eluting stents.

Key facts

Study ID

NCT01794065

Run by

Medstar Health Research Institute

People needed

500

Starts

2012-10-01

Last updated by the study team

2014-08-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients, male or female, 18 years or older;
• Patients with de-novo coronary lesions and slated to receive a Promus Element stent;
• Patients who are slated to undergo IVUS after stent deployment during implantation procedure

You may not qualify if…

• Patients receiving more than one drug-eluting stent within the same lesion during implantation procedure;
• Patients with in-stent restenosis;
• Patients who had IVUS imaging attained with manual pullback.

Where it is running

• Medstar Washington Hospital Center — Washington D.C., District of Columbia, United States

Full record on ClinicalTrials.gov

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