RIAPRE - Non-interventional Registry of Anticoagulation Treatment (BI-006-IT)

NCT00317343 | Withdrawn DMC

• 1 other identifier: BI-006-IT
• Study Type: observational
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

RIAPRE is a non-interventional registry to be settled in Italy with the purpose of collecting data on 600 cases of high risk elective percutaneous coronary intervention (PCI) patients treated with an anticoagulation regime different from unfractionated heparin in monotherapy. About thirty catheterization laboratories will co-operate in this activity. The long term outcome of patients will be taken into consideration. The availability of these data will allow for a better understanding of the therapeutic needs in this area.

Conditions

Coronary Disease

Keywords

Patients candidate to a PCI with a planned anticoagulation regime other than unfractionated heparin in monotherapy

Interventions

Bivalirudin (thrombin specific anticoagulant) DRUG

Percutaneous Coronary Intervention

Eligibility Criteria

• Age: 18 Years - 90 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Primary care clinic

You may qualify if:

• Medical condition or disease to be studied: age \> 18 years.
• Patients are candidates for a PCI with a planned anticoagulation regime other than unfractionated heparin in monotherapy. Taking into consideration the national and international guidelines for this area and the registered indications of the drugs currently used for this purpose it is predicted that the patients will probably receive one of the following:
• unfractionated heparin as an intravenous (IV) bolus followed by IV bolus + infusion of a GPI (abciximab, tirofiban or eptifibatide); or
• bivalirudin as an IV bolus followed by IV infusion, as per the pertinent Summary of Product Characteristics (SPCs).
• Having provided an informed consent (to anonymous data treatment).
• The allocation of any individual patient to the category of "high risk" elective PCI will be made independently and autonomously by the caring physician. However, it is recommended to consider the suitability of patients on the basis of these indicative elements:
• age \> 75 years.
• known diabetes mellitus (type I or type II).
• known renal insufficiency, i.e. serum creatinine \> 1.8 mg or glomerular filtration rate (GFR) \> 60 ml/min (calculated with the Cockroft formula).
• multivessel or complex procedure.
• planned stent on a bifurcation.
• planned stent \> 6 cm long.
• PCI on a degenerated venous bypass: in this particular case a distal protection device should always be used.
• non ST elevation acute coronary syndrome with a PCI planned later than 72 hours after the diagnosis without clinical instability (= "cooled" non ST elevation acute coronary syndrome). This type of patient is considered to be essentially stable and his/her level of risk can be comparable to the risk of patients who are candidates for elective PCI with additional risk factors as listed above.

Sponsors & Collaborators

• Nycomed: lead

MeSH Terms

Conditions

Coronary Disease

Interventions

bivalirudin

Condition Hierarchy (Ancestors)

Myocardial Ischemia; Heart Diseases; Cardiovascular Diseases; Vascular Diseases

Study Officials

• Nycomed Clinical Project Management

  Headquarters

  STUDY CHAIR

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: PROSPECTIVE
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: March 30, 2006
• First Posted: April 24, 2006
• Study Start: March 1, 2006
• Study Completion: February 1, 2008
• Last Updated: May 7, 2012

Record last verified: 2012-05