Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12613000418774
Ethics application status
Approved
Date submitted
7/04/2013
Date registered
15/04/2013
Date last updated
3/09/2019
Date data sharing statement initially provided
3/09/2019
Type of registration
Prospectively registered

Titles & IDs
Public title
Effects of Galvus (Vildagliptin) on Markers of Inflammation in Diabetic Foot Ulcer: A prospective, randomized, double-blind, placebo-controlled pilot study
Scientific title
Effects of Galvus (Vildagliptin) on interleukin-6 in Diabetic Foot Ulcer
Secondary ID [1] 282265 0
Nil Known
Universal Trial Number (UTN)
Trial acronym
GIED
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Type 2 Diabetes
Diabetic Foot Ulcer 288792 0
Anti-inflammatory effects of Vildagliptin 288793 0
Diabetic foot ulcer healing properties of Vildagliptin 288794 0
Condition category
Condition code
Metabolic and Endocrine 289151 289151 0 0
Diabetes

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Arm 1: (Intervention group) will be on oral Metformin 500 mg to 3000 mg per oral in single or divided dosages (2 or 3 times a day) plus Vildagliptin 50 mg to 100 mg per day also to be administered orally for 12 weeks. The dosages of both medications will be determined based on blood glucose levels with the aim of achieving average fasting blood glucose of <7 mmol/l and post-prandial blood glucose of 10 mmol/l or below. Improved adherence will be enhanced by weekly clinic visit and drug tablet return as well as monitoring blood glucose control and progress of the diabetic foot ulcer.
Intervention code [1] 286891 0
Treatment: Drugs
Comparator / control treatment
Arm 2: (Comparator group) will be on given Metformin as described above plus Placebo comprising of lactose 50 mg to 100 mg per day to be taken orally for 12 weeks. The placebo will be identical in appearance to Vildagliptin without the active ingredient.
Control group
Placebo

Outcomes
Primary outcome [1] 289261 0
Significant (20%) reduction of serum levels of IL-6.

IL-6 will be quantified using the Multiplex FlowCytomix system (Bendermedsystems). Antibody-coated beads will be incubated with either patient serum, followed by a biotin-conjugated secondary antibody and finally streptavidin-PE. The sample will be run on BD caliber. Analysis will be performed using software provided by the manufacturer.
Timepoint [1] 289261 0
The IL-6 will be determined and compared at onset (week 1) and 12 weeks.
Secondary outcome [1] 302120 0
a) Partial or complete closure of foot ulcer.

Weekly measurement of the ulcer at the start (week 1) and week 12.
Timepoint [1] 302120 0
Week 1 compared with week 12.
Secondary outcome [2] 302261 0
b) Worsening of the foot ulcer beyond Wagner grade 2.

Weekly assessment of the ulcer throughout period of the study.
Timepoint [2] 302261 0
Week 1 compared with week 12.
Secondary outcome [3] 302262 0
c) Requirement for limb or toe amputation.

Clinical assessment requiring the amputation throughout the 12-week period of the study.
Timepoint [3] 302262 0
Week 1 compared with week 12.
Secondary outcome [4] 302263 0
d) Reduced levels of serum hsCRP, TNF-alpha, IL-1beta, platelet reactivity and significantly raised levels of adiponectin and tissue TGF- beta-1.

These will be quantified using the Multiplex FlowCytomix system (Bendermedsystems). Antibody-coated beads will be incubated with either patient serum, followed by a biotin-conjugated secondary antibody and finally streptavidin-PE. The sample will be run on BD caliber. Analysis will be performed using software provided by the manufacturer.
Timepoint [4] 302263 0
Week 1 compared with week 12.

Eligibility
Key inclusion criteria
1) Subjects >= 18 years of age diagnosed with diabetes (type 1 or 2) on diet only or any diabetic medication regime.
2) Existing diabetes index foot ulcer grade A1 or higher according to the University of Texas Wound Classification System of Diabetic Foot Ulcers on the day of study inclusion. A foot ulcer is defined as any full thickness skin defect existing for at least 14 days. In patients with multiple diabetic foot ulcers the index foot ulcer is defined as the foot ulcer with the largest wound area at the time of inclusion.
3) A suboptimal HBA1c >=7.0% documented somewhere in the patient source documents within 12 weeks prior to study inclusion or on the day of study inclusion.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Exclusion criteria will comply with local label
2. Clinical infection at the studied ulcer site (bacterial and fungal)
3. Planned surgical intervention for the DFU
4. Hypersensitivity to either of the study drug components
5. History of lactic acidosis
6. Type 1 diabetes
7. Current HbA1c <7 or >9%
8. Current Insulin treatment.
9. Active treatment with GLP-1 or other DPP4i medication
10. Use of thiazolidinediones, statins, anti-inflammatory or anti-platelet agents
11. Clinically significant lower-extremity ischemia (as defined by an ankle/brachial index of <0.65)
12. Significant medical conditions that would impair wound healing will also be excluded from the study. These conditions include hepatic, respiratory or cardiac failures, aplastic anemia, scleroderma and malignancy, treatment with immunosuppressive agents or steroids, myocardial infarcts, stroke, major surgery within 6 months of the study, usage of tobacco
13. Severe non-proliferative or proliferative diabetic retinopathy.
14. Active Charcot's foot as determined by clinical and radiographic examination
15. Ulcer of a non-diabetic pathophysiology (e.g., rheumatoid, radiation-related, and vasculitis-related ulcers, calciphylaxis or dystrophic calcinosis cutis)
16. Active malignancy other than basal cell carcinoma as well as subjects with cancerous or pre-cancerous lesions in the ulcer area
17. Renal dysfunction: eGFR <60 ml/min
18. Chronic inflammation (inflammatory bowel disease, inflammatory or rheumatoid arthritis)
19. Pregnancy, lactation or child-bearing potential
20. Recent venous thromboembolism
21. Inability to comply with study protocol

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
All subjects who fit the selection criteria will be invited to participate, and if willing will be provided with information on the study and participant consent will be obtained and then randomized. Patients in each stratum will be assigned numbers using a central stratified randomization scheme.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomization list will be prepared by an independent statistician by the method of computer-generated random numbers for each treatment. Randomization will be carried out following a 2-week period of stabilization on Metformin mono-therapy as described above. Patients will be randomized to treatment with Vildagliptin + Metformin therapy or Metformin + Placebo therapy. This study will be blinded to both patients and treating personnel. All laboratory tests, the major study endpoints, will be performed by professionals blinded to treatment allocation. An interim analysis will be performed after the recruiting 50% of proposed study participants.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Efficacy
Statistical methods / analysis
The objective of this trial is to study the effects of Vildagliptin therapy on inflammatory markers in subjects with diabetic foot ulcer. We plan to prospectively enrol 50 patients with proven diabetic foot ulcer and randomize them in a 1:1, ratio to vildagliptin + metformin or placebo + metformin. We expect to show an improvement (defined as >20% serum IL-6 reduction between the baseline and 3-month assessment) that comprise the primary end point in at least 50% of the patients randomized to Vildagliptin and Metformin therapy and in <10% of the patients randomized to Metformin and Placebo therapy. Furthermore, the proposed sample size was calculated to demonstrate a significant improvement in the intervention group compared to the control group with at least 80% power and a two-sided 5% type 1 error. These requirements will be met with a sample size of 44 patients and a 1:1 randomization design to allow for an approximate dropout rate of 10%, 50 patients will be recruited: this will result in approximately 25 patients in the Vildagliptin + Metformin -intervention group and in the Placebo + Metformin -control group.

The data from the study will be pooled and summarized with respect to demographic and baseline characteristics and efficacy and safety observations. Exploratory analyses will be performed using descriptive statistics. Data will be presented for the complete intent-to-treat population (all patients having taken at least one dose of study medication) as well as the per-protocol population (all patients who completed the study without major protocol deviations).

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
1/08/2013
Actual
23/05/2014
Date of last participant enrolment
Anticipated
6/09/2019
Actual
Date of last data collection
Anticipated
6/12/2019
Actual
Sample size
Target
50
Accrual to date
48
Final
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 842 0
The Townsville Hospital - Douglas
Recruitment postcode(s) [1] 6662 0
4814 - Douglas

Funding & Sponsors
Funding source category [1] 287035 0
Commercial sector/Industry
Name [1] 287035 0
Novartis Pharmaceuticals
Country [1] 287035 0
Australia
Primary sponsor type
Individual
Name
Assoc. Professor Usman H. Malabu; FRCPI, FRACP.
Address
School of Medicine and Dentistry
James Cook University & Townsville Hospital
100 Angus Smith Drive
Douglas, Townsville
QLD 4814.
Country
Australia
Secondary sponsor category [1] 285813 0
None
Name [1] 285813 0
Address [1] 285813 0
Country [1] 285813 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 289069 0
Townsville Hospital Human Research and Ethics Committee
Ethics committee address [1] 289069 0
Ethics committee country [1] 289069 0
Australia
Date submitted for ethics approval [1] 289069 0
15/04/2013
Approval date [1] 289069 0
30/07/2013
Ethics approval number [1] 289069 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 39062 0
A/Prof Usman H. Malabu
Address 39062 0
Department of Endocrinology and Diabetes
Townsville Hospital
100 Angus Smith Drive
Douglas
Townsville
QLD 4814
Country 39062 0
Australia
Phone 39062 0
+61-7-4433 1111
Fax 39062 0
+61-7-4433 2239
Email 39062 0
[email protected]
Contact person for public queries
Name 39063 0
Usman H. Malabu
Address 39063 0
Department of Endocrinology and Diabetes
Townsville Hospital
100 Angus Smith Drive
Douglas
Townsville
QLD 4814
Country 39063 0
Australia
Phone 39063 0
+61-7-4433 1111
Fax 39063 0
+61-7-4433 2239
Email 39063 0
[email protected]
Contact person for scientific queries
Name 39064 0
Usman H. Malabu
Address 39064 0
Department of Endocrinology and Diabetes
Townsville Hospital
100 Angus Smith Drive
Douglas
Townsville
QLD 4814
Country 39064 0
Australia
Phone 39064 0
+61-7-4433 1111
Fax 39064 0
+61-7-4433 2239
Email 39064 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
Deidentified, individual participant data underlying published results only
When will data be available (start and end dates)?
Beginning 3 months and ending 5 years following main results publication
Available to whom?
researchers who provide a methodologically sound proposal
Available for what types of analyses?

for IPD meta-analyses, etc.
How or where can data be obtained?
[email protected]


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
4248Study protocol  [email protected]
4249Ethical approval  [email protected]
4250Statistical analysis plan  [email protected]



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseEffects of vildagliptin on wound healing and markers of inflammation in patients with type 2 diabetic foot ulcer: a prospective, randomized, double-blind, placebo-controlled, single-center study.2022https://dx.doi.org/10.1186/s13098-022-00938-2
N.B. These documents automatically identified may not have been verified by the study sponsor.