Non-Healing Ulcers Without Critical Limb Ischemia

NCT ID: NCT01666093

Last Updated: 2012-08-16

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2015-08-31

Brief Summary

Background: Lower limb arterial revascularization procedures, either percutaneously or surgically performed, are an established treatment modality of ischemic foot ulcers, especially in the setting of a critical limb ischemia. Many other lower limb ulcers are secondary to a combined disease, which may include a concomitant venous disease (chronic venous insufficiency or varicous disease) or a micro-angiopathic disease (i.e. small vessel disease). In this setting, and especially in the absence of a concomitant severe macro-angiopathic disease, the safety and efficacy of a percutaneous lower limb revascularization have so far never been evaluated in a prospective study.

Aim: This study is aimed to evaluate the safety and the efficacy of an endovascular revascularization approach of the lower limb, in all consecutive patients presenting with a non-healing ulcer associated with a mild to moderate peripheral artery disease (i.e. mixed-origin ulcers).

Material and methods: This prospective study will consecutively include all patients presenting with a non-healing ulcer. Included patients must have all the concomitant ulcer co-factors being adequately treated for at least 6 months. Accordingly, an underlying venous disease, infectious disease or inflammatory disorder must be previously evaluated and adequately treated (i.e. compression stocking, varices stripping, antibiotics, local ± systemic anti-inflammatory, etc.). Furthermore, a non-invasive arterial evaluation must be obtained in all patients. The arterial screening must included an ankle-brachial index (ABI) and toe pressure (TP) measurements, a trans-cutaneous oxygen measurement (tcPO2) at the foot and calf levels and a non-invasive arterial mapping (i.e. angio-CT or angio-MRI). This arterial work-up must be compatible with the presence of a mild to moderate peripheral artery disease without any sign or criteria suggesting the presence of a critical limb ischemia.

End-points: The success rate of perform an endovascular revascularization intervention in all consecutive patients which qualify according to the inclusion criteria (technical feasibility). Establish the proportion of procedural related complications (safety). Analyze the clinical and the para-clinical improvements in term of heal of the ulcers, as well as the improvement of the ABI, TP, tcPO2 at 1 week, 1-3-6 months after the procedure (efficacy).

Sample size: The investigators plan to include ≈ 30 patients in two years. After 1 year of enrollment the investigators will perform an interim analysis and will decide at that moment, according to the observed end-points, if prolonging the study would be of any scientific value or if the study has to be interrupt earlier because of a significant improvement of all already treated ulcers.

Detailed Description

see above

Conditions

Peripheral Artery Disease Without Critical Limb Ischemia

Keywords

peripheral artery disease; endovascular procedure; non-healing ulcer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

revascularization group

patients will revascularized after a conservative treatment failure of at least 4 weeks

Group Type: OTHER

Angioplasty of the lower limbs vessels

Intervention Type: PROCEDURE

Standard revascularization techniques will be used in the study

Interventions

Angioplasty of the lower limbs vessels

Standard revascularization techniques will be used in the study

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Patients need to be at least 18 years old

2. Patients have to be admitted to the university hospitals of Geneva for a non-healing lower limb ulcer.

• Eligible patients are those presenting with non-healing lower limb ulcers for more than 3 months.
• Patients will be hospitalized in the Dermatology inpatient clinic.
• Patients had to benefit from at least one thin skin autograft at the ulcer level in the past or during the index hospitalization.

3. Before inclusion in the study, patients must undergo complete angiological diagnostic work-up including:

• A baseline ABI, toe pressure and tcPO2 measurements,
• A non-invasive arterial imaging including an angio-CT scan or an angio-MRI,

4. The non-invasive arterial work-up must revel mild to moderate PAD, without any criteria or sign of CLI (see flow-chart):

• Ankle pressure ≥ 50 mmHg,
• + ABI: < 0.9 or > 1.3,
• ± Toe pressure : 30-100 mmHg
• ± tcPO2: 20-40 mmHg,
• At this moment the patient may be included in the study protocol.

5. All patients presenting with mild to moderate PAD and evidence of at least 1 impaired arterial vessel targeting the ulcer will initially undergo conservative impatient clinic care for at least 2-4 weeks and benefit from at least 1 thin skin autograft.

• Persisting surface of lower limb ulcers will be assessed 1 month later:

-- In the presence of a healed ulcer surface > 70%, the patient will undergo 6 months of clinical follow up at 1-3-6 months.

1. In case of persistence of healed ulcer surface > 70% clinical success will be achieved.

2. In presence of healed ulcer surface < 70% the patient will undergo a new angiological work-up.

• If mild to moderate PAD will be again outlined the patient will join the < 70% healed ulcer group.
• On the other hand, if CLI will be pointed out lower limb revascularisation and at least one thin skin autograft will be performed.

-- In presence of a healed ulcer surface < 70%, endovascular PTA and at least one thin skin autograft will be performed. The ulcers healing will then be monitored at 1-3-6 months and persisting ulcers surface re-assessed:

• in presence of an healed ulcer surface > 70% clinical success will be achieved,
• if presence of an healed ulcer surface < 70% clinical failure will be retained.

Exclusion Criteria

1. Patients who refused to give their written informed consent.

2. Patients, in whom the angiological work-up shows the presence of a CLI, mandating a revascularization procedure attempt (i.e. ankle pressure < 50mmHg, toe pressure < 30mmHg, tcPO2 < 20mmHg) (see particular situation n°2).

3. Patients who do not present with peripheral artery disease (i.e., ABI > 0.9 - < 1.3, TP > 100mmHg, tcPO2 > 40mmHg).

4. Patients in whom the angiological-dermatological work-up shows the presence of another reversible cause of the non-healing ulcer:

• Special attention will be given to the presence of a treatable venous insufficiency (e.g. compression stocking, varices stripping), an underlying inflammatory/infectious process (treatable with antibiotics or topic-systemic antiinflammatory medications) or other reversible mechanical factors (unadapted shoes, etc.).

5. Patients without any significant lesion of the arterial tree (ilio-femoro-popliteal and infra-popliteal):

• In case there will be a single BTK vessel disease not perfusing the ulcer area (e.g. pre-tibial ulcer with a significant stenosis of the posterior tibial artery which does not perfuse the ulcer region), the patient will not be included in the study because any significant ulcer improvement would be expected from this non-target vessel revascularization.

6. Patients in whom the scheduled revascularization procedure will be judged too risky for the patient's safety:

• Chronic kidney failure (= Creatinin Clearance < 20ml/min) with an increased risk of contrast induced nephropathy,
• Too complex arterial disease or anatomy, in which the estimated procedural technical success rate is < 50% (i.e. complex chronic total occlusion).

7. Patients in whom an amputation is unavoidable, despite any revascularization attempt (e.g. extensive skin necrosis [Rutherford class 6]), - If, it will be estimated that, a successful revascularization procedure may reduce the level of amputation, or if a successful intervention may improve the amputation's healing process, the patient may be included in the study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Geneva

OTHER

Sponsor Role: lead

Responsible Party

Robert F Bonvini

MD

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Angiology and Dermatology Divisions / HUG

Geneva, Canton of Geneva, Switzerland

Site Status: RECRUITING

Countries

Switzerland

Central Contacts

Robert F Bonvini, MD

Role: CONTACT

Phone: 0041 22 372 72 00

Email: robert.bonvini@hcuge.ch

Neda Badaoui-Barouti, MD

Role: CONTACT

Phone: 0041 22 372 33 11

Email: neda.badaoui-barouti@hcuge.ch

Facility Contacts

Robert F Bonvini, MD

Role: primary

Other Identifiers

NAC 12-025

Identifier Type: OTHER

Identifier Source: secondary_id

NEWLI-Trial

Identifier Type: -

Identifier Source: org_study_id