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D-Dimer Vs Serial Compression Ultrasound Study

Evaluation of the Safety, Efficacy and Cost-Effectiveness of Two Strategies for the Diagnosis of Deep Vein Thrombosis

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00182351
Enrollment
810
Registered
2005-09-16
Start date
1996-04-30
Completion date
1999-07-31
Last updated
2006-09-08

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

Conditions

Deep Vein Thrombosis

Keywords

deep vein thrombosis, d-dimer, serial compression ultrasound

Brief summary

To determine whether d-dimer testing can be used to simplify and reduce the costs of the diagnostic approach to patients with clinically suspected deep vein thrombosis

Interventions

PROCEDURED-dimer
PROCEDURESerial Compression Ultrasound

Sponsors

Health Canada
CollaboratorOTHER_GOV
Hamilton Health Sciences Corporation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* first suspected deep vein thrombosis * no previous venous thromboembolism * referred to thromboembolism outpatient clinic

Exclusion criteria

* comorbid condition limiting survival to less than six months * contraindication to venography (contrast allergy, etc.) * receiving long term warfarin therapy * receiving full dose heparin therapy for more than 48 hours * absence of symptoms during the five days immediately prior to presentation * symptoms of pulmonary embolism * pregnancy * geographic inaccessibility which precludes follow-up

Design outcomes

Primary

MeasureTime frame
safety of withholding anticoagulants

Secondary

MeasureTime frame
deep vein thrombosis
pulmonary embolism
death

Countries

Canada

Outcome results

None listed

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