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Deep Venous Thrombosis Screening in the ICU by Nurses

E

Emergency Medical Service of the Central Bohemian Region, Czech Republic

Status

Completed

Conditions

Deep Venous Thrombosis

Treatments

Diagnostic Test: Compression ultrasound testing

Study type

Observational

Funder types

Other

Identifiers

NCT03707665
2018-01

Details and patient eligibility

About

Despite of preventive measures, the incidence of deep venous thrombosis (DVT) in ICU patients is estimated to range from 5-31%. While clinical diagnostics is unreliable, ultrasound compression test (UCT) has proven to be a highly sensitive and specific modality for the recognition of lower extremity DVT. Delegating this competence to ICU nurses can increase UCT availability and enable preventive DVT screening. Therefore, the investigators decided to conduct a clinical study to evaluate the sensitivity and specificity of UCT performed by general ICU nurse in ICU patients compared to an investigation by ICU physician certified in ultrasound. Prior to the study, each nurse-investigator participating in the study undergo one-hour training in UCT and examine 5 patients under supervision. Then, ICU patients without known DVT will be investigated by UCT in the femoral and popliteal region of both lower extremities by trained general ICU nurse-investigators. On the same day, the examination will be repeated by an ICU physician-investigator. The results of the examinations of each patient will be blinded to each other for both investigators until both tests are performed. The sensitivity and specificity of the test performed by general nurse will be calculated in comparison with the examination by a specialist.

Enrollment

115 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all ICU patients without known deep venous thrombosis, hospitalised more than 72 hours

Exclusion criteria

  • contraindication of compression ultrasound testing
  • end-of-life decision regimen of care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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