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Molecular and Cellular Mechanisms of the In-stent-thrombosis

Molecular and Cellular Mechanisms of the In-stent-thrombosis. Is it Possible to Predict a In-stent-thrombosis Using Biomarkers?

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00652015
Enrollment
0
Registered
2008-04-03
Start date
2008-05-31
Completion date
2010-05-31
Last updated
2015-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients With SAT or LT After Stent Implantation (PCI)

Keywords

in-stent-thrombosis, CD39, CD73, EPC

Brief summary

In-Stent-Thrombosis is a rare but serious complication after implantation of stents during PTCA.

Detailed description

In this prospective, open, not-randomized, controlled single-center pilot study 80 patients having had an in-stent-thrombosis (40 sub-acute thromboses (SAT), 40 late thromboses (LT)) and a control group of 80 patients having not developed a thrombosis will be compared. The aim of this study is the establishment of diagnostic markers vor prediction of SAT (detection of CD39- and CD73-activity, respectively)and of LT (EPC-number and function, respectively) correspondingly aiming at the early identification of patients with high risk for developing an in-stent-thrombosis.

Interventions

None listed

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients having developed an SAT or LT after stent implantation using PTCA

Exclusion criteria

* instabel coronary heart diseases, * systemic autoimmune diseases, * rheumatic diseases, * tumors, * impaired kidney or liver function, * surgery within the last 3 months, * pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
The aim of this study is to establish diagnostic markers for prediction of SAT and LT, respectively, by identification of CD39 and CD73-activity and EPC-number and function, respectively.may 08 to may 2010

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026