Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05112705

Diagnosing Deep-vein Thrombosis Early in Critically Ill Patients

Led by King Abdullah International Medical Research Center · Updated on 2025-09-19

1800

Participants Needed

1

Research Sites

193 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The DETECT randomized controlled trial addresses the question of whether surveillance ultrasound in critically ill patients by facilitating DVT detection reduces the incidence of PE and lowers all-cause 90-day mortality. The primary outcome is 90-day all-cause mortality.

CONDITIONS

Official Title

Diagnosing Deep-vein Thrombosis Early in Critically Ill Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Medical, surgical, or trauma ICU patients aged 18 years or older
  • Patients expected to stay in the ICU for more than 2 calendar days
Not Eligible

You will not qualify if you...

  • Patients diagnosed with deep vein thrombosis or pulmonary embolism within the last year
  • Patients receiving chronic systemic anticoagulation
  • Patients currently receiving therapeutic doses of anticoagulants such as UFH or LMWH
  • Patients who cannot have adequate ultrasound on lower limbs due to burns, lacerations, infections, ischemia, large dressings, or amputation
  • Patients with an Inferior Vena Cava (IVC) filter
  • Known or suspected pregnancy
  • Patients with life support limitations, life expectancy under 7 days, or receiving palliative care
  • Patients previously enrolled in the DETECT trial within the last 180 days
  • Patients enrolled in another trial where co-enrollment is not allowed

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

King Abdulaziz Medical City

Riyadh, Riyadh Region, Saudi Arabia, 11426

Actively Recruiting

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Research Team

Y

Yaseen M Arabi

CONTACT

H

Haifa Al Humeidi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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