Skip to main content
OpenTrials
Completed

NCT Number: NCT02222376

Effect of Topic Pirfenidone in Diabetic Ulcers

Pirfenidone is a synthetic molecule, which acts as a potent modulator of the effect of various cytokines (TNF-α, transforming growth factor-β, platelet derived growth factor and vascular endothelial growth factor, among others) that possesses anti-inflammatory and anti-fibrinolytic properties.

The aim of this study is to compare the effect of topic treatment with pirfenidone compared to conventional treatment in chronic diabetic foot ulcers.

The hypothesis is that treatment with topic pirfenidone in chronic diabetic foot ulcers (Wagner 1 to 2) reduces the ulcer size and shortens the healing time compared to conventional treatment. This is a randomized, controlled and crossover study. Patients will be randomly assigned to conventional treatment or topic pirfenidone for eight weeks. At the end of this period they will change groups. Each week ulcers will be for size, depth, length and evidence of infection. The ulcers will have proper debridement in the conventional treatment group and debridement plus topical pirfenidone application in the pirfenidone group. Subjects will be instructed to do daily ulcer cleansing and for those in the topical pirfenidone group, in addition to cleansing they will be instructed to apply the gel twice a day.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Mexico City, 14000, Mexico

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Men or women
  • Type 1 or 2 diabetes
  • Age ≥ 18 years
  • Wagner 1 or 2 diabetic foot ulcer
  • Diabetic ulcer for more than 8 weeks duration
  • Willing to participate in the study with signed informed consent

Exclusion criteria

  • Ankle/brachial index < 0.4 (critic ischemia)
  • Use topical or systemic antibiotics
  • Inability to attend to the weekly evaluations
  • Inability to do daily ulcer cleansing
  • Autoimmune diseases
  • Active pharmacologic topical or systemic ulcer treatment
  • Treatment with immunosuppressors such as steroids, radiotherapy, chemotherapy
  • Pregnancy or lactation

Treatment and study plan

pirfenidone

Drug

Twice a day topical application

Other names: Kitoscell Q

Debridement

Procedure

Weekly ulcer debridement

Primary outcomes

  1. Ulcer size

    Time frame: 16 weeks

Other outcomes

  1. Healed ulcers

    Time frame: 16 weeks

  2. Adverse effects

    Time frame: 16 weeks

  3. Healing time

    Time frame: 16 weeks

Sponsors and collaborators

Lead sponsor

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Other

Registry information

Official study title

Effect of Treatment of Diabetic Foot Ulcers With Topic 8% 1-phenyl-5-methyl-2-[1h]-Pyridone (Pirfenidone) Combined With Modified Disulfur Diallyl Oxide (Odd-m) in Gel.

Acronym: PirDFI

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Aug 21, 2014
Registry last updated
Feb 15, 2016

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.

Published trials that share one or more normalized conditions with this study.