Diagnosing deep vein thrombosis early in critically ill patients (DETECT) trial: a protocol for a randomised controlled trial.
Yaseen M Arabi, Farhan Alenezi, Fahad Al-Hameed...
https://pubmed.ncbi.nlm.nih.gov/41161824Actively Recruiting
Led by King Abdullah International Medical Research Center · Updated on 2025-09-19
1800
Participants Needed
1
Research Sites
39 weeks
Total Duration
This trial investigates whether using twice weekly surveillance ultrasound to detect deep vein thrombosis (DVT) early in critically ill patients can reduce pulmonary embolism (PE) and lower the risk of death within 90 days. It is an open-label, randomized controlled study conducted across multiple centers and countries, focusing on patients admitted to intensive care units (ICU). Participants who qualify will be randomly assigned to either receive ultrasound scans of both lower limbs twice a week or receive standard care without routine ultrasound. The ultrasound is done to detect DVT early and is performed according to the study schedule or treating team discretion. The study compares outcomes between these two groups. During the study, patients will be monitored for up to 90 days, with assessments including ultrasound scans, clinical evaluations for PE and bleeding, and survival status. The main measurement is all-cause mortality at 90 days. Secondary outcomes include the occurrence of proximal DVT within 28 days or until ICU discharge, pulmonary embolism during hospital stay up to 28 days, and clinically important bleeding events up to 90 days. The study involves screening patients within 48 hours of ICU admission and follows them through their hospital stay and beyond as needed.
CONDITIONS
Diagnosing Deep-vein Thrombosis Early in Critically Ill Patients
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - Within the first 48 hours of ICU admission
Participants are screened for eligibility to participate in the trial.
1 screening visit (in-person)
Duration - Up to 28 days or until ICU discharge, whichever comes first
Participants are monitored with twice weekly bilateral lower limb ultrasound or standard care as per treating team discretion.
Twice weekly visits for ultrasound or standard care
Duration - Up to 90 days after randomization
Participants are observed for clinical outcomes including mortality and bleeding events.
Total: 1 location
1
King Abdulaziz Medical City
Riyadh, Riyadh Region, Saudi Arabia, 11426
Actively Recruiting
Y
Yaseen M Arabi
H
Haifa Al Humeidi
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
2
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Yaseen M Arabi, Farhan Alenezi, Fahad Al-Hameed...
https://pubmed.ncbi.nlm.nih.gov/41161824