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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00450528
Other study ID # StV 31-2006
Secondary ID
Status Completed
Phase N/A
First received March 21, 2007
Last updated October 23, 2007
Start date February 2007
Est. completion date October 2007

Study information

Verified date October 2007
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Federal Office of Public Health
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate the natural kinetics of D-dimers that occur after abdominal surgery.


Description:

Venous thromboembolism (VTE) is a potentially fatal disease with an estimated incidence of 0.1%. One third of the VTE occur as pulmonal embolism with a mortality up to 25% (White RH. Circulation 107:2003)

Serum d-dimer levels are used as sensitive marker for the diagnosis of VTE (Kelly J et al. Arch Intern Med, 162: 2002). Because of its sensitivity, the determination of serum D-dimer levels is an accepted method to exclude VTE in the outpatient setting meaning that VTE may be excluded in case of normal D-dimer levels (Kelly J. Lancet 359: 2002). The specificity of the D-dimer testing, however, is low. This is true especially in the postoperative phase. The interpretation of elevated D-dimer levels in surgical patients remains elusive.

The natural kinetics of D-dimers after surgery is not known. The question to what extent D-dimer levels rise after surgery and how long it may take D-dimer levels to return to normal after surgery is not yet determined. This information is needed to be able to use D-dimer testing for VTE diagnosis in surgical patients.

In this study, D-dimer levels are measured in surgical patients immediately before (day 0) and repeatedly after surgery. D-dimer level measurement will be stopped after D-dimer levels returned to normal.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date October 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- patients undergoing elective surgery

Exclusion Criteria:

- age < 18 years

- patients not speaking german

- patients involved in another study

- pregnancy

- concommitant inflammatory disease

- patients with oral anticoagulation

- patients having received fresh frozen plasma

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms

  • Natural Kicetics of d-Dimers After Surgery

Locations

Country Name City State
Switzerland Univeryity Hospital, Clinic for Visceral- and Transplantation Surgery Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland,