Current partner codePEPTIDESDE
NCT01011504·Not applicable·OBSERVATIONAL

Utilisation of Angiox® in European Practice

Status

Completed

Phase

Not applicable

Enrollment

2,019

Locations

2

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

The objective of this study is to determine utilisation patterns in patients receiving Angiox® in participating European centres. Additionally, through the collection of descriptive safety and outcomes data, this study will contribute to the Risk Management strategy for Europe

Interventions

Treatment arms and agents.

No intervention details reported.

Timeline

From registration to results.

  1. First posted

    Nov 11, 2009

  2. Study start

    May 2009

  3. Primary completion

    Oct 2010

  4. Study completion

    Dec 2010

  5. Results posted

    Not reported

  6. Registry updated

    Jan 19, 2012

Outcomes

What the study measures.

Primary outcomes

Posology and usage patterns of Angiox®: Dose(s) and time of bolus and infusion administered

Time frame · from hospital admission until hospital discharge, or 7 days after administration (which ever is earlier).

Secondary outcomes

Death Myocardial infarction Unplanned revascularisation Stroke Major* and minor bleeding Thrombocytopenia Stent thrombosis Adverse events and serious adverse events

Time frame · measured in-hospital (prior to discharge), and at post-hospital discharge in outpatient as per local practice (30 days)

Eligibility

Who can take part.

Minimum age
Not reported
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Eligible for, and receive treatment with Angiox®. * Willing and able to provide written informed consent to the use of their data in accordance with relevant local Data Protection laws, policies and regulations Exclusion Criteria: * Participation in other interventional clinical research studies involving the evaluation of investigational drugs, including Angiox®, or devices at the time of enrolment. * Patients not eligible for treatment for Angiox®.

Study locations

2 registered sites.

France · Germany. Showing up to 24 locations stored in the fast local snapshot.

Centre Hospitalier Universitaire de Caen

Caen, France

Medizinische Klinik I Kardiologie/Pneumologie/Internistische

Rostock, Germany

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Bivalirudin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.