Tissue Monitoring During Endovascular Intervention (TIME)

Pedra Technology

Status: Unknown

Conditions: Peripheral Artery Disease; Arterial Occlusive Diseases; Peripheral Arterial Disease

Study type: Observational

Funder types: Industry

Identifiers

NCT04744870

CIP-002

Details and patient eligibility

About

Tissue perfusion assessment is key to more accurate measurement of foot ischemia, which is in turn an important factor in appropriate treatment decisions. In practice though, tissue perfusion measurements are not routinely undertaken as few practical solutions exist that are easy to use and fit in everyday clinical practice. Pedra has developed a novel, easy to use, non-invasive device that can be used in practice to better inform treatment decisions.

Full description

Tissue perfusion assessment is key to more accurate measurement of foot ischemia, which is in turn an important factor in appropriate treatment decisions. In practice though, tissue perfusion measurements are not routinely undertaken as few practical solutions exist that are easy to use and fit in everyday clinical practice. Pedra has developed a novel, easy to use, non-invasive device that can be used in practice to better inform treatment decisions.

This is a feasibility study to demonstrate the ability of the Xauron system to track tissue perfusion changes in patients undergoing endovascular intervention for the treatment of peripheral artery disease (PAD). The findings of this study are for research purposes and will also be used to help with the future education of physicians about the potential use of the Xauron system. In addition, this early pilot data will be used to help power larger, more definitive studies relating to the intra-procedural use of the Xauron system.

Enrollment: 80 estimated patients

Sex: All

Ages: 40 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• The subject is undergoing endovascular intervention for the management of their PAD.
• The subject is between 40 and 90 years of age.
• Documented lower limb arterial occlusive or stenotic disease (using ankle-brachial index / pulse volume recording, duplex ultrasound or CT angiogram) within the last 8 weeks.
• In the opinion of the Investigator, the subject is willing and able to comply with the protocol and complete all protocol assessments.
• Subject has been informed of the nature of the study, agrees to its provisions and has willingly provided written informed consent, approved by the appropriate Institutional Review Board (IRB)

Exclusion criteria

• Subjects on an investigational drug or being treated with an investigational therapeutic device, within 30 days of the study visit, that in the view of the Investigator might interfere with the study outcomes.
• Presence of a condition that the Investigator considers will compromise the subject's ability to participate in the study.
• Subjects on renal replacement therapy
• Signs of active infection causing localized inflammation on the plantar or dorsal surfaces of the foot.
• Diabetic subjects with a Charcot neuropathic osteoarthropathy
• Lack of intact skin, or pathological skin conditions, at the proposed sensor pad positions that may impair or prevent the adherence of medical adhesives in general.