Iontophoresis of Treprostinil to Enhance Wound Healing in Diabetic Foot Skin Ulcers

Diabetic Foot Ulcer Clinical Trial

— InTREPiD  

Official title:

Iontophoresis of Treprostinil to Enhance Wound Healing in Diabetic Foot Skin Ulcers

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03654989
• Other study ID #: 38RC17.163
• Status: Terminated
• Phase: Phase 1/Phase 2
• Start date: January 28, 2020
• Est. completion date: December 7, 2021

Study information

• Verified date: December 2023
• Source: University Hospital, Grenoble
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Assess the effect of iontophoresis of treprostinil on wound closure over 12 weeks, in patients with DFU.

In the present study the investigators aim at establishing the proof-of-concept of iontophoresis of treprostinil as a potential treatment of diabetic foot ulcers in humans. The main hypothesis is that in patients with DFUs, the pharmacodynamic effect of a PGI2 analogue potentiates the effect of low-intensity current on microvascular function, tissue oxygenation and healing.

Description:

Diabetic foot ulcers (DFUs) represent a serious public health problem associated with significant morbidity and health costs. Despite optimal etiologic treatment and local care, amputation is frequent, stressing the need for new treatments. Tissue ischemia is the primary cause for nonhealing DFUs. The cutaneous microcirculation, by providing tissue perfusion, fluid hemostasis, and delivery of oxygen and nutrients, plays a critical role in the pathophysiology and impaired healing of DFUs.

The investigators therefore hypothesize that the skin microcirculation, and more specifically the prostacyclin (PGI2) pathway, is an interesting target for the local treatment of DFUs. Indeed, besides its potent vasodilator effect, PGI2 plays a role in the promotion of fibroblast migration and angiogenesis in wound models.

However, the benefit of systemic (i.e. IV or SC) treatments is counterbalanced by potentially serious vasodilatation-induced side effects (e.g. severe headaches, flushing, tachycardia and hypotension). These properties are dose-limiting and are associated with safety issues and increased costs. The paradox is that impaired microvasculature prevents the drug, when administered intravenously, from diffusing properly to the wound. Elevated doses are therefore needed, leading to adverse drug reactions.

The originality of this approach is to locally deliver negatively charged PGI2 analogues into and around the wound under the influence of a low-intensity current, through a method called iontophoresis. Iontophoresis enables a controlled delivery of ionized drugs into/through the skin under the influence of low-intensity current. In addition, endogenous electrical signals in the wound are known to play a role in healing, by increasing the directed migration of keratinocytes, fibroblasts and neutrophils. Exogenous electric stimulation would mimic this phenomenon with a positive impact on wound healing. In summary, both the drug and its vehicle could therefore work synergistically, while delivering the drug locally therefore limiting side effects due to systemic diffusion.

This is a prospective, monocentric, controlled, randomized, double-blinded phase I/II study The main objective is to assess the effect of iontophoresis of treprostinil on wound closure over 12 weeks, in patients with DFU. The investigators will compare wound closure, expressed as the percentage change of the wound area over time (12-week follow-up), between 3 groups: iontophoresis of treprostinil, iontophoresis of placebo, and standard of care. Wound area will be assessed with a digital camera and image analysis software.

Secondary objectives are:

• To assess the effect of iontophoresis of treprostinil on complete healing over 3 months

• To assess the effect of iontophoresis of treprostinil on the time to complete healing

• To assess the effect of iontophoresis of treprostinil on skin perfusion at the site of the ulcer and around the wound

• To evaluate the effect of iontophoresis of treprostinil on skin oxygenation around the lesion and on healed skin

• To assess the pharmacokinetics (PK) of topical administration of treprostinil over damaged (wounded)

• To evaluate the safety of the procedure

The study will be divided into two consecutive parts:

Part 1: 8 to 24 patients with DFU (depending on the total number of doses tested, and the number of doses per patient) will be included in a single ascending dose (SAD) safety study of treprostinil iontophoresis.

Part 2: 36 patients with DFU associated with microvascular dysfunction (+/- neuropathy) will be randomized into three groups to receive either: 1. Treprostinil iontophoresis; 2. Placebo iontophoresis; 3. Standard care. Drug administration (placebo or treprostinil), but not standard care, will be double-blind. After a 10-day treatment, follow-up includes 6 visits over 10 weeks.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 4
• Est. completion date: December 7, 2021
• Est. primary completion date: December 7, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with type 2 diabetes according to the criteria of the American Diabetes Association (ADA), with one or more foot ulcer of microvascular or mixed etiology:

• The ulcer size must be =1 cm² and <20 cm²

• Grade 1A, 1C, 2A or 2C (University of Texas Classification of Diabetic Foot)

• Patient affiliated to social security insurance or beneficiary of social security insurance.

Exclusion Criteria:

• History of hypersensitivity reaction to treprostinil

• Pulmonary veno-occlusive disease (PVOD)

• Systemic treatment with any PGI2 analogue in the past two months.

• Critical ischemia of the lower limb, defined as leg pain at rest associated with ankle pressure <50 mmHg.

• Infected wound, treated with antibiotics in the past 15 days.

• Active or uncontrolled cardiovascular disease as follows:

• Myocardial infarction, or angina within 6 months of study participation

• Arrhythmia (uncontrolled, highly symptomatic, requires treatment or life-threatening).

• Congestive heart failure.

• Stroke or transient ischemic attack within 3 months of study participation

• Uncontrolled hypertension: systolic blood pressure> 180 mmHg or diastolic blood pressure> 105 mmHg (2 abnormal readings during visit)

• Valvular heart disease

• Severe liver disease (Child-Pugh C) at the time of enrollment

• Active gastroduodenal ulcer

• Intracerebral hemorrhage

• Trauma or any clinical event susceptible to be responsible for hemorrhage within 6 months of study participation

• Renal disease (creatinine > 2 mg/dL and/or estimated glomerular filtration rate<30 mL/min, history of dialysis)

• Unstable diabetes that has resulted in hyperosmolar coma or ketoacidosis, and/or documented increase or decrease in HbA1c of more than 2.0% within the previous 3 months.

• Pregnancy or Lactation

• Females of childbearing potential not using an effective form of birth control as determined by the investigators.

• Participant involved in another interventional clinical study

• Person deprived of liberty by judicial order

• Person under guardianship or curatorship

Related Conditions & MeSH terms

• Diabetic Foot
• Diabetic Foot Ulcer
• Foot Ulcer
• Skin Ulcer
• Ulcer

Intervention

Drug:
• Treprostinil iontophoresis
We will administer treprostinil at increasing doses by a iontophoresis.

Device:
• Remodulin® placebo iontophoresis
Placebo iontophoresis will be performed using Remodulin® placebo (United Therapeutics) delivered with Axion GmbH electrodes connected to a PeriIont generator (Perimed). Part 1: 1 administration/day, on separate days, with 72h between two doses. The intensity will be set at 120 µA during 60 minutes, i.e. a total current of 17.3 mC/cm². Part 2: 1 administration/day for 10 days. The intensity will be set at 120 µA during 60 minutes, i.e. a total current of 17.3 mC/cm².

Locations

Country	Name	City	State
France	CHU Grenoble Alpes	Grenoble

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Comparison of wound closure between the 3 groups: iontophoresis of treprostinil, iontophoresis of placebo, and standard of care, over12 weeks.	Wound closure is expressed as the percentage change non-reepithelialized skin area over time (12-week follow-up), assessed with a digital camera and image analysis software.	Up to 12 weeks
Secondary	The percentage of patients with complete healing at the last follow-up visit	Wound area will be assessed with a digital camera and image analysis software.	week 12
Secondary	Comparison of time to complete healing between groups	Time to complete reepithelialization will be sought in the medical record on a monthly basis.	From date of randomization until the date of documented healing, assessed up to 12 months.
Secondary	The effect of iontophoresis of treprostinil on skin perfusion assessed with laser speckle contrast imaging at the site of the ulcer and around the wound	Cutaneous perfusion will be assessed as cutaneous vascular conductance, and compared between groups	day 9
Secondary	Comparison of skin oxygenation around the lesion and on healed skin (when possible)	Comparison using transcutaneous pressure of oxygen	Day 0 and Day 9 and week 12
Secondary	8-hour PK profile. AUC0-8	8-hour PK profile. AUC0-8 will be calculated from seven time points: immediately after the end of iontophoresis ( T0), 15 min, 30 min, 1h, 2h, 4h, and 8h	part 1 : V1 (day0) V2 (day3 or more after V1) V3 (day3 or more after V2) V4 (day3 or more after V3), Part 2 : at days 0 and 9
Secondary	Incidence of treatment-emergent adverse events, among which hypotension, any cutaneous reaction at the site of iontophoresis, local pain, liver enzymes.	All adverse events will be rated according to the NIH Common Terminology Criteria for Adverse Events.	During all the study, 3 months of follow-up for every subject
Secondary	Evaluation of safety via blood pressure	Blood pressure will be continuously recorded with digital photoplethysmography.	During all the study, 3 months of following for every subject
Secondary	Evaluation of safety via the appearance of the wound	Photographs of the wound will be taken and sent to investigators, blinded to the group	During all the study, 3 months of following for every subject