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Philadelphia, Pennsylvania 19106


Purpose:

The study will look at the safety profile (unwanted effects) of the long-lasting anticoagulant PEG-hirudin (SPP200) and compare these unwanted effects to those of unfractionated heparin, commonly used in haemodialysis to avoid clotting of the graft and of the haemodialysis machine.


Criteria:

- Patients undergoing chronic haemodialysis via an arteriovenous graft - Arteriovenous graft in place for at least 3 months - Duration of haemodialysis of at least 3 months, with 3 full dialysis sessions per week with a duration between 2 and 5 hours per session - Women patients must be either postmenopausal for more than 1 year or, if of childbearing age, must use adequate contraception - Women patients must have a negative serum pregnancy test within one week of randomisation - Able to provide written informed consent prior to study participation


NCT ID:

NCT00074620


Primary Contact:

Study Chair
Jessica M Mann, MD, PhD
Speedel Bio Ltd


Backup Contact:

N/A


Location Contact:

Philadelphia, Pennsylvania 19106
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 14, 2017

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