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Completed

NCT Number: NCT05661474

Fitostimoline® Hydrogel Versus Saline Gauze Dressing in Diabetic Foot Ulcers

Diabetes Mellitus (DM) is one of the most widespread metabolic diseases and the alarming rise in its prevalence worldwide poses enormous challenges. The microvascular and macrovascular complications of DM heavy impact on longevity and quality of life, and in particular diabetic foot ulcers (DFUs) are among the ten top causes of worldwide disease burden and disability Essential components of the standard care, management, and treatment of DFUs are represented by health education, strict control of blood glucose and cardiovascular risk factors, offloading, local debridement, and adequate dressing. A wide variety of dressing is available, and these include basic contact dressings (low adherence dressings such as saline gauze, paraffin gauze or simple absorbent dressings) and advanced dressings (alginate, hydrogel, films, hydrocolloid, foam).

It is important underline that due to lack of evidence from head-to-head randomized controlled trials (RCTs), the relative effects of any of these dressings in DFUs remain unclear. Consequently, so far clinical evidence supporting the choice for either hydrogel or saline gauze dressing, has been related mostly on clinician perception rather than high quality evidence. Here we evaluated the efficacy and safety of Fitostimoline® hydrogel dressing versus saline gauze dressing in patients with DFUs in a monocentric, two-arm, open-label, randomized, controlled trial.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Department of Clinical Medicine and Surgery Federico II University

Naples, 80131, Italy

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Type 1 diabetes and type 2 diabetes,
  • adult patients with DFUs at Grades IC or IIC for a period of at least 12 weeks,
  • an akle brachial index >0.8,
  • be able to understand simple instructions,
  • provided voluntary, signed informed consent

Exclusion criteria

  • active infection
  • evidence of ischaemia in the limb,
  • osteomyelitis,
  • gangrene,
  • systemic inflammatory or autoimmune disease,
  • use of corticosteroids, immunosuppressive agents, radiation therapy and chemotherapyan,
  • known hypersensitivity to any of the dressing components.

Treatment and study plan

Fitostimoline ® hydrogel group

Drug

Treatment of DFUs with Fitostimoline® hydrogel every day for 12 weeks.

Saline gauze group

Drug

Treatment of DFUs with saline gauze every day for 12 weeks.

Primary outcomes

  1. the proportion of patients complete responders

    Time frame: 12 weeks

    The primary outcome was the proportion of patients that at the end of study period of 12 weeks (V6) were categorized as complete responders -complete healing of the wound defined as reepithelialisation of 100% without medications.

Sponsors and collaborators

Lead sponsor

Federico II University

Other

Registry information

Official study title

The Effects of Fitostimoline® Hydrogel Versus Saline Gauze Dressing in Patients With Diabetic Foot Ulcers: a Monocentric, Two-arm, Open-label, Randomized, Controlled Trial.

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Dec 22, 2022
Registry last updated
Dec 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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