Efficacy of the Combination of Isosorbide Dinitrate Spray and Chitosan in Diabetic Foot Ulcers
Primary Purpose
Diabetic Foot Ulcers
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Chitosan
Isosorbide dinitrate
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Diabetic Foot Ulcers focused on measuring diabetic foot ulcers, chitosan, isosorbide dinitrate spray
Eligibility Criteria
Inclusion Criteria:
- Patients with diabetic foot ulcers in grade I and II of the classification of Wagner
- with leg arm index> 0.8 and
- without specific treatment for foot ulcers referred to the experimental and clinical
Exclusion Criteria:
- Patients with another type of topical medication
- patients with diabetic foot ulcers in grade III and
- with leg arm index <0.8
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Chitosan
Isosorbide dinitrate spray
Placebo
Arm Description
Chitosan chemically is a high-molecular-weight linear polycationic heteropolysaccharide comprising copolymers of 1,4-linked D-glucosamine and N-acetyl-D-glucosamine
Isosorbide dinitrate spray (2.5 mg) is an organic nitrate, is a vasodilator with effects on both arteries and veins. The chemical name of ISDN is 1,4:3,6-dianhydro-D-glucitol 2,5-dinitrate.
Placebo in the same pharmacological presentation
Outcomes
Primary Outcome Measures
Biopsies
Histological changes in ulcers
Secondary Outcome Measures
Full Information
NCT ID
NCT02789033
First Posted
March 24, 2015
Last Updated
December 17, 2020
Sponsor
University of Guadalajara
1. Study Identification
Unique Protocol Identification Number
NCT02789033
Brief Title
Efficacy of the Combination of Isosorbide Dinitrate Spray and Chitosan in Diabetic Foot Ulcers
Official Title
Efficacy of the Combination of Isosorbide Dinitrate Spray and Chitosan in Diabetic Foot Ulcers
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
June 2015 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Guadalajara
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The prevalence of diabetic foot ulceration in the diabetic population is 4-10%; the condition is more frequent in elder patients. It is estimated that about 5% of all patients with diabetes present a history of foot ulceration, while the lifetime risk of diabetic patients developing this complication is 15%. The majority (60-80%) of foot ulcers will heal, while 10-15% of them will remain active, and 5-24% of them will finally lead to limb amputation within a period of 6-18 months after the first evaluation , 2 out of 3 patients with a limb amputation could also be involved in a new amputation in the next year; higher or in the other leg , Eighty-five percent of lower-limb amputations in patients with diabetes are preceded by foot ulceration. The management of chronic diabetic foot ulcers (DFU) suggests multi-disciplinary approaches including control of diabetes, orthotic shoe wear, off-loading device, wound care and surgery in selected cases. However, treatment of DFU remains challenging because of unsatisfactory results from surgical and non-surgical treatments. Many adjunctive therapies are designed to improve the care of DFU including negative pressure wound therapy , ultrasound, recombinant human platelet-derived growth factor-BB (rPDGF-BB) Hyperbaric oxygen and acellular matrix product among others.
Detailed Description
A randomized, placebo controlled, double-blind Clinical trial was designed. 60 Patients with diabetic foot ulcers in grade I and II of the classification of Wagner, with leg arm index> 0.8 and without specific treatment for foot ulcers referred to the experimental and clinical Therapeutic Institute will be included. All patients give written informed consent; previously the protocol was approved for the bioethics committee of the CUCS, of the Guadalajara University, registration number 030-2010. Patients with another type of topical medication will be excluded. Isosorbide dinitrate spray (2.5 mg).
Preparation of chitosan Hydrogels: The composition of gel formulation will be given prior training. ISDN and chitosan gel will be applied handled under aseptic conditions to the wound, and covered with sterile bandages. The patients will be evaluated every 2 weeks (macroscopic study and measurement of the ulcerated area) until 6 views. A second biopsy will be done one week before the finalization of the treatment of 15 weeks. The biopsies will be embedded on paraformaldehyde (4%) and paraffin. Sections of 5 µm were analyzed by a pathologist to determine hypertrophic and hyperplasic capillaries, inflammation and cellular matrix using Hematoxylin & eosin and Masson's trichrome stains. An immunohistochemical stain was also realized to evaluate several molecular markers such as α-SMA (abcam, Cambridge, MA), Desmin (abcam, Cambridge, MA), VEGF (abcam, Cambridge, MA) and Von Willebrand Factor (Chemicon, CA). (figure 1) Statistical analysis: It will be done using SPSS program for Windows Version 10.0, the results of quantitative variables were expressed in average and standard deviation. The differences between baseline and subsequent pharmacologic intervention measurements will be investigated with the Wilcoxon test. The Mann Whitney U test will be used to compare groups. Frequencies by categories as well as percentages will be quantified for qualitative variables. Comparisons between groups were performed with Chi2. For all comparisons p < 0.05 will be considered as significant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcers
Keywords
diabetic foot ulcers, chitosan, isosorbide dinitrate spray
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
68 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Chitosan
Arm Type
Active Comparator
Arm Description
Chitosan chemically is a high-molecular-weight linear polycationic heteropolysaccharide comprising copolymers of 1,4-linked D-glucosamine and N-acetyl-D-glucosamine
Arm Title
Isosorbide dinitrate spray
Arm Type
Active Comparator
Arm Description
Isosorbide dinitrate spray (2.5 mg) is an organic nitrate, is a vasodilator with effects on both arteries and veins. The chemical name of ISDN is 1,4:3,6-dianhydro-D-glucitol 2,5-dinitrate.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo in the same pharmacological presentation
Intervention Type
Drug
Intervention Name(s)
Chitosan
Other Intervention Name(s)
polymers
Intervention Description
Chitosan chemically is a high-molecular-weight linear polycationic heteropolysaccharide comprising copolymers of 1,4-linked D-glucosamine and N-acetyl-D-glucosamine
Intervention Type
Drug
Intervention Name(s)
Isosorbide dinitrate
Other Intervention Name(s)
organic nitrate
Intervention Description
Isosorbide dinitrate (ISDN), is an organic nitrate, is a vasodilator with effects on both arteries and veins. The chemical name of ISDN is 1,4:3,6-dianhydro-D-glucitol 2,5-dinitrate
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Magnessium Calcuim
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Biopsies
Description
Histological changes in ulcers
Time Frame
75 days
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients with diabetic foot ulcers in grade I and II of the classification of Wagner
with leg arm index> 0.8 and
without specific treatment for foot ulcers referred to the experimental and clinical
Exclusion Criteria:
Patients with another type of topical medication
patients with diabetic foot ulcers in grade III and
with leg arm index <0.8
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leonel Garcia, PhD
Organizational Affiliation
University of Guadalajara
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
22529027
Citation
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Citation
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Links:
URL
http://www.hindawi.com/journals/ecam/2013/243568/
Description
The outcome of management of diabetic foot ulceration (DFU) is poor and insufficient. DFU therapy includes the standard management as debridement of the wound, revascularization procedures,off-loading of the ulcer and antibacterial actions,
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Efficacy of the Combination of Isosorbide Dinitrate Spray and Chitosan in Diabetic Foot Ulcers
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