HELP-Apheresis in Diabetic Ischemic Foot Treatment (H.A.D.I.F)

Condition(s) targeted: Foot Ulcers; Arteriosclerosis Obliterans; Diabetes Mellitus

Intervention: LDL-apheresis (Device)

Phase: N/A

Status: Recruiting

Sponsored by: Universita di Verona

Official(s) and/or principal investigator(s):
Maria Grazia Zenti, MD, Principal Investigator, Affiliation: Division of Endocrinology and Metabolic Diseases, University Hospital of Verona
Enzo Bonora, MD, PhD, Study Director, Affiliation: Division of Endocrinology and Metabolic Diseases, University Hospital of Verona

Overall contact:
Maria Grazia Zenti, Email: mariagrazia.zenti@univr.it

Diabetic foot (DF) is a common, severe and costly complication of diabetes. DF is underlied by neuropathy, atherosclerosis of distal arteries and infection, which result in tissue ulcers and necrosis. Alterations in microcirculatory function and in blood rheology may concur in causing tissue damage. In recent years there has been accumulating evidence that LDL apheresis (LA) does not only reduce cholesterol but also has a series of pleiotropic effects that improve the microcirculation, increasing peripheral tissue perfusion. HADIF is a randomized, multicentric, prospective clinical study aimed at assessing the effect of LDL apheresis treatment in association with traditional therapy for ulcers, in patients with an ischemic diabetic foot ulcer (class I and II Texas Wound Classification System)and peripheral vasculopathy not susceptible to revascularization. A total of 132 patients will be enrolled. Participants will be centrally randomized to receive traditional therapy alone (TT) or in association with LA. TT includes standard medication of ulcers, antiaggregant therapy and statins. LA will be performed with HELP system, for a total of 10 sessions in 9 weeks. The primary end-point of the study is ulcer healing; secondary endpoints include improvements of peripheral oxygenation, resolution of pain, reduction of circulating inflammatory markers, cardiovascular events during one year's follow-up. This clinical Study has been approved by local EC on 25 may 2011 (Study number 1953). TO BE NOTED: since diabetic patients in our "Diabetic-Foot UNIT" often presented foot ulcers more severe than class II Texas, a formal amendment has been submitted to EC for recruiting patients with diabetic foot ulcer of class III Texas. The amendment was already approved on 5 may 2012.

Official title: HELP-Apheresis in Diabetic Ischemic Foot Treatment (H.A.D.I.F): a RCTrial to Evaluate the Effect of LDL-apheresis on the Recovery of Diabetic Ulcers in Patients With Peripheral Vasculopathy Not Susceptible to Revascularization.

Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome: Proportion of subjects obtaining the ulcer healing (Class 0A according to TEXAS classification) after 12 month from the study starts.

Secondary outcome:

Improvement of the peripheral oxygenation evaluated by means of transcutaneous oximetry measurement at foot level: TcP O2 (mmHg).

Evaluation of pain level variation (verbal numeric range; score from 1 to 10)

Lowering of circulating inflammation markers (C Reactive Protein, Fibrinogen). CRP plasmatic concentration (mg/L) and fibrinogen (g/L)

Rate of cardiovascular events in the observation period (1-year follow-up).

proportion of subjects with minor amputation (only toe or part of the foot removed)- in agreement with the approved amendment

proportion of subjects with major amputation (these are usually below the knee or above the knee)- in agreement with the approved amendment

Detailed description: Aim of the protocol is to evaluate the effect of LDL-apheresis in combination with traditional therapy, on the recovery of diabetic ulcers in patients suffering from diabetic ischemic foot and peripheral vasculopathy that cannot be revascularized. Patients who qualify for the study will be randomized to the traditional treatment combined to apheresis (Experimental Arm) or to the standard treatment only (control Arm). The randomization stratified according to the lesion gravity level (class TEXAS I vs II vs III),allocation 1: 1. The randomization list will be generated by the statistic software "Stata 11". The lists of randomization (one list for each class TEXAS ) will be generated and will be stored by the coordinator centre. When a patient satisfies the study inclusion criteria, will be contacted the coordinator centre (by phone/mail) for group allocation. 132 patients will be enrolled (66 patients in experimental arm, 66 patients in control arm). Traditional Therapy (TT) includes standard medication of ulcers, antiaggregant therapy and statins. LDL-apheresis (intervention Arm) will be performed with HELP system, for 10 session in 9 weeks. Blood samples will be collected (at basal, and after 3-6-9-12 months) in order to determine the following parameters: glycaemia, insulin, glycated haemoglobin, microalbuminuria/creatinuria,CBC, fibrinogen, total cholesterol, HDL-cholesterol, LDL-cholesterol, Triglycerides, Lp(a), C-reactive protein (CRP), pentraxin3 (PTX3). Furthermore, in patients of experimental arm, blood samples will be collected at basal and at the end of LDL-apheresis sessions no. 2 and 10 in order to determine CBC, fibrinogen, total cholesterol, HDL-cholesterol, LDL-cholesterol, Triglycerides, Lp(a), CRP, PTX3 (time schedule, after 1 and 9 weeks). The value of the lab tests obtained at the end of apheresis will be normalized due to a possible hemodilution, according to the following formula:

F dil= (1 - Htc pre-apheresis) / ( 1 - Htc post-apheresis). Xcorrect = Xmeasured * Fdil.

Ulcer evaluation: staging according to Texas Wound classification System and ulcer surface evaluation (diameter, mapping of the lesions by means of drawing their profiles on Opsite film; digital picture): at basal, at 9th week and after a 3-6-9-12 month follow-up. The ulcers evolution will be "in blind" monitored by an evaluator who will check ulcer-map and digital picture without knowing to which randomization arm they belong. Transcutaneous oximetry: basal, at 4th week (i. e. after the 5th apheretic session). at 9th week (at the end of the 10 apheresis sessions) and after the next 3-6-9-12 month follow-up. Questionnaire on quality of life (SF36): basal, at 9th week (at the end of the 10 apheresis sessions) and after the next 6-12 month follow-up. Pain intensity rate (verbal numeric range) basal, at 9th week (at the end of the 10 apheresis sessions) and after the next 3-6-9-12 month follow-up. Doppler flowmeter : basal, at 9th week (at the end of the 10 apheresis sessions) and in the subsequent follow-up at 6 and 12 months.

Minimum age: 18 Years. Maximum age: 80 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Diabetic patients

- Ischemic diabetic ulcers (class I, II and III Texas Wound Classification System);

- documented peripheral vasculopathy with at least a previous event of failed

revascularization (no ulcer healing). Exclusion Criteria:

- Patient refusal to participate

- BMI > 35 kg/m2

- Ischemic diabetic ulcers class III Texas Wound Classification System

- Patients presenting a bleeding diathesis, malignant tumor, heart failure not allowing

extracorporeal technique.

- Haemodialysis

Maria Grazia Zenti, Email: mariagrazia.zenti@univr.it

universita Verona, Verona 37100, Italy; Recruiting
Maria Grazia Zenti, MD, Phone: +39 0458123745, Email: mariagrazia.zenti@univr.it

Starting date: February 2012
Last updated: December 18, 2014