WIREDUP: Wearable Insoles for Recurrent Diabetic Ulcer Prevention

Diabetes Clinical Trial

— WIREDUP  

Official title:

Prevention of Foot Ulcer Recurrence in Individuals Who Are at High-risk for Diabetic Foot Complications Using the Orpyx SI Sensory Insole System: a Multisite, Randomized, Controlled Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05950659
• Other study ID #: WIREDUP
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 1, 2024
• Est. completion date: June 1, 2027

Study information

• Verified date: July 2023
• Source: Orpyx Medical Technologies Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary aim of this study is to demonstrate the impact of the Orpyx® SI Sensory Insoles (Orpyx Medical Technologies Inc., Calgary AB, Canada) ("Orpyx" or "the Company") as an adjunct to the standard of care (SOC), as compared to SOC alone, on reducing plantar ulceration incidence in individuals who are at risk for developing diabetic foot complications.

The secondary aims of this study are to evaluate participant quality of life, participant engagement, and economic impact, including cost-effectiveness and cost-utility. The study will also use the unique data set collected (plantar pressure, temperature, step count, movement and adherence feedback) to identify foot-loading histories that either lead to or prevent the development of ulceration in the diabetic foot.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 500
• Est. completion date: June 1, 2027
• Est. primary completion date: January 1, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosed Type 1 or 2 diabetes

• Clinically diagnosed neuropathy via Neuropathy Monofilament Test

• Qualification as a "high-risk participant," meaning a recent history (<12 months) of a healed diabetic neuropathic ulceration on the weight-bearing surface of one or both feet (this includes the plantar distal toe surface)

• Complete healing of any previous foot ulcers, as defined by complete re-epithelialization of that ulcer which is confirmed by two medical exams that occur at least two weeks apart (V0 and V1)

• Ability to walk independently (without use of wheelchair) for 30 steps. Use of a walker or cane is acceptable as long as the participant can walk for at least 30 steps.

• Aged >18 years

• Ability to understand all study requirements and have a life expectancy greater than the study duration

• Vascular assessment (i.e., ABI, segmental pressure) that demonstrates the participant has adequate lower extremity perfusion

• Subject is willing and able to maintain the required offloading (as applicable for the location of the healed ulcer)

• Subject is willing and able to wear the Orpyx Sensory Insoles during ambulatory activity and at home during waking hours, and for a minimum of 5 hours per day

• Compatibility of the device with the participant's footwear

• Most recent HbA1c level of < 12.0% (in the last 12 months)

• Amputations, if present, are compatible with the use of insoles

Exclusion Criteria:

• Active ulcer or presence of other open chronic wound (on foot or other body surface), regardless of etiology (e.g., vasculitis, neoplasms, or hematological disorders)

• History of known non-neuropathic foot ulcer (e.g., arterial, or venous insufficiency ulcer)

• Presence of severe vascular disease (refer to acceptable ABI parameters in inclusion criteria)

• Dementia

• Psychiatric illness or social situations that would limit compliance with the study

• Serious underlying balance dysfunction, regardless of etiology

• Significant cardiopulmonary or other systemic disease limiting the participant's ability to walk at least 30 steps or to stand for an amount of time equal to or greater than five (5) minutes

• Current participation in another clinical investigation of a medical device or a drug; or participation in such a study within 30 days prior to study enrolment

• Osteomyelitis or gangrene of the lower extremity

• Uncorrected plantar Charcot neuroarthropathy

• Bunion which would predispose ulcer formation (clinician discretion)

• Extreme equinus

• Hallux valgus

• Hallux rigidus / limitus

• HbA1c levels >= 12%

• At the start of V1, and prior to randomization, the subject no longer meets the entrance criteria (inclusion and exclusion)

• Any condition that would affect or limit the ability to properly fit both shoes with the device under study

• Subject has a history of intercurrent illness or conditions that would compromise the safety of the subject or their ability to participate in the study

• Amputations on the foot which the clinician deems incompatible with the insoles (i.e., those that require additive insole modifications)

Related Conditions & MeSH terms

• Diabetes
• Diabetic Foot
• Diabetic Foot Ulcer
• Foot Ulcer
• Peripheral Nervous System Diseases
• Peripheral Neuropathy
• Ulcer

Intervention

Device:
• Orpyx SI Sensory Insole System
The Orpyx SI Sensory Insoles System uses Orpyx Sensory Technology: a powered limb overload warning technology intended for monitoring physiologic parameters, such as plantar pressure, temperature, motion, and adherence, and providing real-time cues for pressure offloading

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Orpyx Medical Technologies Inc.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Plantar ulcer recurrence		12 months