Diabetic Foot Ulcer Study Comparing Cytal Wound Matrix 1-Layer to Standard of Care

Diabetes Mellitus, Type 2 Clinical Trial

Official title:

A Prospective, Randomized, Controlled Trial Comparing Cytal Wound Matrix 1-Layer to Standard of Care (SOC) in the Management of Diabetic Foot Ulcers (DFUs)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03626623
• Other study ID #: CR2017-006
• Status: Terminated
• Phase: N/A
• Start date: May 21, 2019
• Est. completion date: February 18, 2020

Study information

• Verified date: August 2021
• Source: Integra LifeSciences Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a two-armed randomized controlled trial (RCT) primarily aimed at determining if application of Cytal Wound Matrix 1-Layer intervention to diabetic foot ulcers shows improved wound closure rates when compared to standard care intervention.

Description:

This is a prospective, two-armed, multi-center randomized controlled trial (RCT) comparing Cytal Wound Matrix 1-Layer intervention to standard of care (SOC) intervention in patients presenting with diabetic foot ulcers (DFU). Up to one hundred and fifty patients recruited from US based medical centers and randomized (using a 2(active):1(control) randomization scheme) to receive either Cytal Wound Matrix 1-Layer intervention or standard of care intervention.Complete wound closure incidence, wound healing rates, wound recurrence, and various health related quality of life (HRQOL) outcomes will be compared between study arms. Additionally, a cost effective analysis (i.e. direct and indirect costs) and review of individual and group changes in narcotic prescription patterns will also be evaluated. While incidence of wound closure rates will be evaluated through 12 weeks, protocol defined patient follow-up is for two years.

Data will be captured for remaining study objectives during these two years. An independent biostatistician will review all participant data for power and futility analysis. In addition, a clinical events committee (CEC) will adjudicate all adverse events (AEs) and serious adverse events (SAEs).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 15
• Est. completion date: February 18, 2020
• Est. primary completion date: February 18, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

1. Provision of signed and dated informed consent form by subject or legally authorized representative.

2. Stated willingness to comply with all study procedures and availability for the duration of the study. Subject is able and willing to tolerate non-removable offloading device for the duration of the run-in and intervention phases of the study.

3. Subject is male or female and at least 21years of age.

4. Subject has a clinical diagnosis of type 1 or type 2 diabetes.

5. Subject's current foot ulcer(s) has been present for > 30 days and = 365 days.

6. Subject's current foot ulcer(s), post-debridement is/are predominantly below the malleoli and on the plantar surface of the foot.

7. Subject's foot ulcer(s) must be Wagner type 1 or type 2.

8. Post debridement, subject's ulcer(s) are free of necrotic debris and appear to be comprised of healthy, vascularized tissue.

9. All qualifying ulcers are = 5cm away from any other ulcer on the same foot.

10. Subject's ulcer(s) is = 1cm2 and = 20cm2 at randomization (length x width).

11. Subject's HbA1C reading is =10%.

12. Subject's Serum Creatinine = 3.0mg/dL.

13. Subject has adequate circulation to the foot as measured by Ankle-Brachial Index (ABI) = 0.7.

14. Negative pregnancy test at randomization for women.

Exclusion Criteria:

An individual who meets any of the following criteria will be excluded from participation in this study:

1. Subject is pregnant, breastfeeding, or unwilling to practice birth control during participation in the study, if applicable.

2. Allergy or hypersensitivity to materials in porcine-based study products (per subject report) or personal preference.

3. Subject report of concurrent participation in another clinical trial that involves a drug.

4. The subject has any condition that, in the Investigator's opinion, would warrant exclusion from the study or prevent the subject from completing the study.

5. Subject has clinical evidence of gangrene on any part of the affected foot.

6. The subject's ulcer(s) is/are due to a non-diabetic etiology, ulcers of arterial, venous stasis, pressure, radiation, traumatic, rheumatoid, vasculitis, collagen vascular disease, or other non-diabetic etiologies.

7. Subject has unstable Charcot foot, Charcot foot with a bony prominence(s) or Charcot amputation.

8. Qualifying wound(s) is connected to another ulcer via a fistula.

9. Subject has one or more medical condition(s) including: renal, hepatic, hematological, neurologic, or immune disease that in the opinion of the Investigator would make the subject an inappropriate candidate for this wound healing study.

10. Subject has or has had a malignant disease (other than basal cell carcinoma) that has not been in remission for at least five years.

11. Subject is receiving oral or parenteral corticosteroids, immunosuppressive or cytotoxic agents, or is anticipated to require such during the course of the study.

12. Subject has acute osteomyelitis of the affected foot.

13. Subject's ulcer(s) is accompanied by active cellulitis.

14. Subject has received growth factor or enzymatic therapy within 2 weeks of consent.

15. Subject is currently receiving or has received radiation, radiologic implants, or chemotherapy.

16. Subject is allergic to any of the primary or secondary dressing materials, including occlusive dressings and the adhesives on such dressings.

17. Subject's ulcer(s) has decreased in size by >30% during the run-in phase.

18. Subject's ulcer(s) has increased in size by >50% during the run-in phase.

19. Subject's ulcer(s) has tunnels or sinus tracts that cannot be completely debrided.

20. Subject has severe malnutrition as evidenced by albumin <2.0 g/dL.

21. Subject has a bleeding disorder as documented by a diagnosis of a bleeding disorder.

22. Subject is on dialysis.

23. Any DFU(s) is infected and has not been treated for any clinically suspected infection prior to application of any product.

Related Conditions & MeSH terms

• Diabetes
• Diabetes Mellitus
• Diabetes Mellitus, Type 1
• Diabetes Mellitus, Type 2
• Diabetic Foot
• Foot Ulcer

Intervention

Device:
• Cytal Wound Matrix 1-Layer
Cytal® Wound Matrix 1-Layer is composed of a porcine (pig) derived extracellular matrix known as urinary bladder matrix. It is intended for the management of a variety of wounds.The individual device is intended for one time use.

Other:
• Standard of Care (SOC)
Standard of care (SOC) is defined as the usual care a licensed health care provider would give patients to treat diabetic foot ulcers or wounds. SOC associated procedures and policies may vary across clinical settings.

Locations

Country	Name	City	State
United States	Limb Preservation Platform, Inc.	Fresno	California
United States	MedStar Health Research Institute	Hyattsville	Maryland
United States	Louisiana State University Health Science Center (LSUHSC)	New Orleans	Louisiana

Sponsors (1)

Lead Sponsor	Collaborator
Integra LifeSciences Corporation

Country where clinical trial is conducted

United States, 

References & Publications (7)

Bann CM, Fehnel SE, Gagnon DD. Development and validation of the Diabetic Foot Ulcer Scale-short form (DFS-SF). Pharmacoeconomics. 2003;21(17):1277-90. — View Citation

Chen YH, DeMets DL, Lan KK. Increasing the sample size when the unblinded interim result is promising. Stat Med. 2004 Apr 15;23(7):1023-38. — View Citation

Dumville JC, O'Meara S, Deshpande S, Speak K. Hydrogel dressings for healing diabetic foot ulcers. Cochrane Database Syst Rev. 2013 Jul 12;(7):CD009101. doi: 10.1002/14651858.CD009101.pub3. Review. — View Citation

Margolis DJ, Kantor J, Berlin JA. Healing of diabetic neuropathic foot ulcers receiving standard treatment. A meta-analysis. Diabetes Care. 1999 May;22(5):692-5. — View Citation

Rice JB, Desai U, Cummings AK, Birnbaum HG, Skornicki M, Parsons NB. Burden of diabetic foot ulcers for medicare and private insurers. Diabetes Care. 2014;37(3):651-8. doi: 10.2337/dc13-2176. Epub 2013 Nov 1. Erratum in: Diabetes Care. 2014 Sep;37(9):2660. — View Citation

Wu L, Norman G, Dumville JC, O'Meara S, Bell-Syer SE. Dressings for treating foot ulcers in people with diabetes: an overview of systematic reviews. Cochrane Database Syst Rev. 2015 Jul 14;(7):CD010471. doi: 10.1002/14651858.CD010471.pub2. Review. — View Citation

Yazdanpanah L, Nasiri M, Adarvishi S. Literature review on the management of diabetic foot ulcer. World J Diabetes. 2015 Feb 15;6(1):37-53. doi: 10.4239/wjd.v6.i1.37. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Wounds With Wound Closure	The primary endpoint of the study is to measure the incidence of complete wound closure (defined as 100% epithelialization) between randomized groups. Number of wounds was calculated as the total across all participants.	up to 12 weeks
Secondary	Wound Size Change	Measure changes in wound size, measured in cm2/week between randomized groups.	up to 12 weeks
Secondary	Complete Wound Closure Time	Measure time to complete wound closure between randomized groups.	up to 12 weeks
Secondary	Wound Recurrence	Measure wound recurrence after healing is complete between randomized groups.	at 26 week visit and 52 week visit
Secondary	Short Form-20 (SF-20)	The Short Form-20 is a 20-item questionnaire used to assess generic health outcomes from the participant's perspective. Scores are linearly measured from 0 (worst) to 100 (best) health functioning scores, respectively.	Baseline visit, visit #7, visit #13, 26 wk. visit, and 52 wk.visit
Secondary	Diabetic Foot Ulcer Scale- Short Form (DFS-SF)	The diabetic foot ulcer scale- short form (DFS-SF) is a 29-item questionnaire designed to assess the impact of diabetic foot ulcers (DFUs) and their intervention on quality of life of participants diagnosed with diabetes. Scores measured from 0 (lower) to 100 (higher) quality of life, respectively.	Baseline visit, 26 week visit, and 52 week visit
Secondary	Visual Analogue Scale (VAS) for Pain	The visual analogue scale (VAS) is a psychometric response scale for pain. It measures subjective characteristics or attitudes regarding perceived pain levels from participants. Participants are asked to draw a vertical line on a 10 cm horizontal line indicating what their current pain level would be. The distance between the start of the horizontal line to the vertical line is calculated in cm with a higher score (100) indicating greater pain intensity.	Up to 52 week visit (until study completion)
Secondary	Katz Index of Independence in Activities of Daily Living (KATZ ADL)	The Katz ADL is a 6-item questionnaire measuring independence in activities of daily living such as bathing, dressing, toileting, transfers, feeding, and continence. Each item is dichotomized as either having a score of zero (i.e. dependence) or one (i.e. independence). This will be completed with the aid of a trained study staff member.	Baseline visit, visit 7, visit 13, 26 wk visit, and 52 wk visit
Secondary	Adverse Events Frequency	This outcome measures diabetic foot ulcer (DFU) related adverse event frequency including unexpected adverse device events (UADEs) or serious adverse experiences (SAEs) throughout the duration of the study as well as evaluate such adverse event frequencies between randomized groups.	up to 52 week visit (until study completion)
Secondary	Narcotic Prescription Changes Between Trial Arms	This outcome measures changes in number of diabetic foot ulcer (DFU) related narcotic prescriptions by study participant and between randomized groups.	up to 52 week visit (until study completion)
Secondary	Participant Ambulatory Status	This outcome measures any changes in ambulatory status (i.e. bed, wheel chair, walk w/ assistance, or walk independent) by study participant and between randomized groups.	up to 52 week visit (until study completion)
Secondary	Return to Work Status	This outcome measures differences in "return to work status" and/or "reported work status", activities of daily living, or disability status by study participant and between randomized groups.	up to 52 week visit (until study completion)
Secondary	Diabetic Foot Ulcer (DFU) Specific Ancillary Medical Care	This outcome measures the incidence of diabetic foot ulcer (DFU) specific related medical care a study participant receives outside of the medical care provided by the investigator. Examples of ancillary care include, but are not limited to, emergency room (ER) visits, urgent care visits, outside medical procedures such as surgery, etc. The incidence of subjects requiring ancillary medical care will be tabulated and compared between randomized groups. This data will be collected via two questions (i.e. "Did participant receive any ancillary medical care?" and "If "yes", then specify where"). Responses are verified using source documentation.	up to 52 week visit (until study completion)
Secondary	Diabetic Foot Ulcer (DFU) Related Direct Product(s) Costs	This outcome measures direct costs of the products by total cost per subject stratified by healed vs. non healed DFU.	up to 52 week visit (until study completion)
Secondary	Indirect Diabetic Foot Ulcer (DFU) Product(s) Costs	This outcome measures total indirect and incidental costs of diabetic foot ulcer products used per study participant by each visit.	up to 52 week visit (until study completion)

External Links

•   Description of Cytal Wound Matrix Products (including Cytal Wound Matrix 1-Layer)