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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06296576
Other study ID # CHM-2023/S49/06
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 1, 2024
Est. completion date May 1, 2026

Study information

Verified date February 2024
Source Centre Hospitalier le Mans
Contact Christelle JADEAU
Phone +33244710781
Email cjadeau@ch-lemans.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Critical Limb Ischaemia (CLI), the final stage of arterial disease, is a therapeutic emergency whose prognosis depends largely on the time taken to diagnose it. The growing prevalence of this condition and the associated healthcare costs make it an important public health objective. Diagnostic criteria for Critical Limb Ischaemia differ between learned societies and countries. Its diagnosis is most frequently based on the combination of a clinical criterion (ischaemic decubitus pain and/or necrotic wounds, with a time to onset > 2 weeks) and a haemodynamic criterion (ankle systolic pressure (ASP) < 50mmHg or toe systolic pressure (TSP) < 30 mmHg or transcutaneous oxygen pressure (TCPO2) < 30 mmHg). Recent studies have highlighted the importance of pulsed Doppler flow analysis in quantifying arteriopathy of the lower limbs, both by systematically analysing flow modulation and by measuring the systolic rise time of distal arteries (dorsal artery of the foot and lateral plantar artery). The main aim of our study is therefore to validate a reliable and accessible diagnostic tool for screening patients suffering from CLI so that they can be referred to a reference centre as early as possible.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 431
Est. completion date May 1, 2026
Est. primary completion date May 1, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years; - Patient referred to the vascular medicine department of one of the investigating centres for arterial Doppler ultrasound of at least one lower limb and for whom a measurement of the systolic pressure index at the toe will be performed. - Presence of proven arterial disease, asymptomatic or not, defined by the presence of one of the following criteria: - Rest ankle systolic pressure index = 0.90 - Rest toe systolic pressure index = 0.70 Exclusion Criteria: - Patient with haemodynamic instability, unable to tolerate a delay in therapeutic management caused by the ultrasound examination and measurement of systolic pressure at the toe; - Patients with surgical management of the lower limb (in relation to lower limb arteriopathy), already scheduled at the time of inclusion. - Patients with a life expectancy of less than 24 hours; - History of transmetatarsal amputation or amputation at a more proximal level compromising the measurement of systolic pressure and occlusion at the toe and/or TCPO2; - Refusal to participate

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
arterial ultrasound scan
An arterial ultrasound scan of the lower limbs with pulsed Doppler analysis of arterial flow spectra over the abdominal aorta, dorsal artery of the foot and lateral plantar artery, bilaterally

Locations

Country Name City State
France Centre Hospitalier de CHOLET Cholet
France Centre Hospitalier du Mans Le Mans

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier le Mans

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the intrinsic diagnostic performance of the maximum systolic rise time (TASmax) in the distal arteries of the foot The diagnosis of Critical Limb ischaemia will be defined by a toe systolic pressure = 30 mmHg 12 months
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