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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06068504
Other study ID # Heating_PAD
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date December 31, 2024

Study information

Verified date November 2023
Source University of Nove de Julho
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study will be to evaluate shear stress and blood flow parameters in lower limb arteries during arm cycle ergometer exercise in participants with peripheral artery disease. Twenty patients participants with peripheral artery disease and claudication symptoms will be recruited. Participants will perform 3 experimental sessions in random order. Iarm-cranking (15 sets of two minutes exercise), warm water foot immersion, and control. During the interventions, blood pressure and heart rate will be assessed every 6 minutes. Measurements of arterial diameter, blood flow, anterograde and retrograde shear stress of the femoral artery will be evaluated using a two-dimensional ultrasound device with spectral Doppler.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 20
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 50 Years to 100 Years
Eligibility Inclusion Criteria: - clinical diagnosis of peripheral artery disease or ankle-brachial index less than 0.90 in one or both limbs - do not present peripheral neuropathy; - be able to exercise after medical approval - aged 50 or over. Exclusion Criteria: - Medication change during the study - Health problems that contraindicates the practice of physical exercise.

Study Design


Intervention

Other:
Arm-cranking exercise
Arm-cranking exercise
Heating
Immersion of the foot in warm water

Locations

Country Name City State
Brazil University Nove de Julho São Paulo

Sponsors (1)

Lead Sponsor Collaborator
University of Nove de Julho

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Femoral artery diameter [mm] Measurements will be obtained through duplex ultrasound in accordance with global recommendations. Before the intervention and at 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, and 30 minutes into the intervention
Primary Femoral artery shear rate [sec.-1] Measurements will be obtained through duplex ultrasound in accordance with global recommendations. Before the intervention and at 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, and 30 minutes into the intervention
Primary Femoral artery Blood flow [mL/min] Measurements will be obtained through duplex ultrasound in accordance with global recommendations. Before the intervention and at 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, and 30 minutes into the intervention
Secondary Brachial systolic and diastolic blood pressure [mmHg] Systolic and diastolic blood pressures will be assessment in the arms with an automatic blood pressure monitor (HEM-742, Omron Healthcare, Japan) Before the intervention and at 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, and 29 minutes into the intervention
Secondary Heart rate [bpm] Heart rate assessment with a heart rate monitor (Polar H10, Polar®, Finland) Before and up to 30 minutes into the intervention
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