Intravascular Ultrasound-Guided Intervention for Venous Leg Ulcers (IGuideU)

Philips

Status: Terminated

Conditions: Venous Ulcer of Leg

Treatments: Diagnostic Test: IVUS; Other: Continued Compression Therapy/Stockings

Study type: Interventional

Funder types: Industry

Identifiers

NCT04696354

200202 (Other Identifier)

IGT_IGD_VLU_2020_10876

Details and patient eligibility

About

This clinical study is a global, prospective, multi-center, randomized controlled trial to determine if the use of intravascular ultrasound (IVUS) as an adjunctive imaging modality and as an interventional treatment guide will result in a more accurate diagnosis of deep vein occlusion (DVO), will guide optimal therapy, and will provide better clinical outcomes with reduced cost of care for patients presenting with persistent venous leg ulcers (VLUs).

Full description

This study will be conducted in 266 subjects presenting with venous ulcers that have previously undergone treatment for superficial of and/or perforator venous disease, if clinically indicated, followed by at least 3 months of prescribed compression therapy prior to screening.

There are 6 study visits for each subject that will be completed over a period lasting approximately 24 months. Subjects will undergo a baseline/screening assessment (visit 1) followed by an interrogation procedure (visit 2) if the subject is enrolled into the interrogation arm. If the subject is randomized to the deferred interrogation arm, he/she will have a hospital/office visit in lieu of the interrogation procedure, which will be considered visit 2. For statistical purposes, the wound assessment performed at the index procedure/hospital visit will be considered the baseline measurement. 30±14 days and 90±14 days after Visit 2, the subject will return to the office for a 1- and 3-month follow-up visit, respectively. The subjects will return at 6- and 12-months post-index procedure/Visit 2 for follow-up assessments. The follow-up period for this study will be approximately 24 months, with a phone call only at 24-months post-index procedure/visit 2.

The clinical study has a planned enrollment period of 36 months and a planned study duration period of 5.17 years

Enrollment: 12 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Be between 18 and 85 years of age.
• Able and willing to participate and comply with the protocol, including the defined follow-up schedule, by signing an Institutional Review Board (IRB) or Ethics Committee approved informed consent form.
• Active venous leg ulcer (CEAP C6).
• Previously completed treatment for clinically significant reflux in the superficial and/or perforator venous system of the target limb at least 3 months prior to enrollment, if clinically indicated.
• Completed at least 3 months of prescribed compression therapy after any ablation.
• Palpable dorsalis pedis or posterior tibial artery (DP/PT) pulses at ipsilateral foot or ankle brachial index (ABI) ≥0.8.
• Be able to ambulate unassisted or with non-motorized assistive devices.
• Current VLU present ≤48 months.

Exclusion criteria

• Patient is known pregnant or breast-feeding or planning to become pregnant in the following year.
• If antiplatelet and anticoagulation therapy cannot be tolerated.
• Previous venous stent implantation involving the target limb, target lesion, or inferior vena cava.
• Previous venovenous bypass surgery involving the target limb.
• Previous endovascular recanalization of the target lesion segment.
• Known metal allergy precluding stent implantation.
• Known or suspected to have inadequate inflow to support stent patency in the target limb.
• Active cancer diagnosis.
• Known positive test for COVID-19 (Sars-CoV-2) within the last 2 weeks and actively symptomatic.
• Known or suspected venous outflow obstruction caused by tumor compression/encasement with or without thrombus.
• Known allergy to contrast media that cannot adequately be pre-medicated prior to study procedure.
• Known renal dysfunction (defined as eGFR <30mL/min/1.73m2) that would preclude adequate contrast usage.
• Diagnosed with right heart failure/pulmonary hypertension.
• Has known clinically significant abnormal platelet count outside laboratory reference ranges.
• Has known clinically significant abnormal white blood cell count (WBC), fever, sepsis or positive blood culture.
• Organ transplant requiring immunosuppressant therapy.
• Unstable angina pectoris, or myocardial infarction within 30 days and/or hemorrhagic stroke within 3 months.
• Subjects with an active diagnosis of osteomyelitis of the ipsilateral limb.
• Previous or planned surgical or catheter-based procedure on index leg within 30 days before or 30 days after the index procedure.
• Active participation in another investigational drug or device study.
• Subject has any condition, which, in the opinion of the investigator, precludes the subject from participation.

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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12 participants in 2 patient groups

Interrogation Arm

Other group

Description:

patients will first be evaluated with MPV (limited to 3 views). The prescribed course of treatment based on the MPV results will be documented and patients will then be evaluated using IVUS. A treatment plan based on IVUS results will be compared with the MPV guided treatment plan and any differences will be documented. Any patients determined to still require venous stenting based on IVUS results will be stented accordingly using IVUS to guide stent placement.

Treatment:

Diagnostic Test: IVUS

Deferred Interrogation Arm

Other group

Description:

Deferred Interrogation Guidelines for this study are as follows: Mandate: • Continued compression therapy/stockings as prescribed. Allow: * Periodic leg elevation. * Sclerotherapy under ulcer bed. * Recommend mechanical debridement as needed. * Wound biopsy if evidence of infection. * Systemic antibiotics if patient is diagnosed with an infection, avoid prophylactic prescription. * Pain management medication (Pentoxifylline/Trental) allowed but not recommended * Topical antimicrobial as needed. Prohibit: * Negative pressure systems. * Artificial and/or autologous skin grafting within first 3 months after randomization and within the first 3 months for subjects that crossover from deferred interrogation to the interrogation arm.

Treatment:

Other: Continued Compression Therapy/Stockings