Status:
RECRUITING
Non-healing Diabetic Foot Ulcers Treated With Standard Care With or Without BR-AM
Lead Sponsor:
BioStem Technologies
Conditions:
Non-infected Diabetic Foot Ulcer
Diabetic Foot
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This trial is a multicenter, randomized, controlled study designed to evaluate the safety and efficacy of BioREtain® Amniotic Membrane (BR-AM) plus standard of care versus standard of care only in the...
Detailed Description
This study examines a patient population with a diabetic foot ulcer (DFU) having adequate perfusion without clinical signs and symptoms of infection. Historical data has demonstrated that around 30% o...
Eligibility Criteria
Inclusion
- Patient has signed the informed consent form.
- Male or female patient at least 18 years of age or older, as of the date of the screening visit.
- Confirmed diagnosis of Type 1 or Type 2 Diabetes.
- Has a DFU that is located below the malleoli at least 1.0 cm2 or up to 20.0 cm2 when measured by the investigator staff at the screening visit using the eKare device post debridement.
- a. If more than one ulcer is present the selected target ulcer must be at least 2 cm from the nearest edge of any adjacent ulcers.
- The depth of the target foot ulcer is graded as Wagner Grade I or II, i.e., with no evidence of exposed muscle, tendon, bone, or joint capsule.
- The target ulcer is "chronic, hard-to-heal," defined as having a duration of \> 4 weeks but ≤ 52 weeks at the time of the screening visit.
- Arterial supply adequacy to the foot with the target ulcer confirmed by any one of the following:
- Great toe pressure ≥ 40 mm/Hg
- Systolic blood pressure Ankle Brachial Index (ABI) in the range ≥ 0.70 ≤ 1.20
- TcPO2 ≥ 30 mmHg from the foot
- Toe Brachial Index or TBI ≥ 0.50
- Willing to follow all instructions given by the Investigator, return for all visits, and adhere to off-loading protocols while on the study.
Exclusion
- Hemoglobin A1c (HbA1c) level is \> 12% (108 mmol/mol).
- Chronic oral steroid use of \> 7.5 mg daily within the previous 30 days preceding screening.
- Chronic oral or parenteral corticosteroids, or any cytotoxic agents within the previous 30 days preceding screening.
- Has tested positive for Human Immunodeficiency Virus (HIV) or has Acquired Immune Deficiency Syndrome (AIDS).
- Has malignancy or history of cancer in 5 years preceding the screening visit other than non-melanoma skin cancer.
- Pregnant women.
- Women of child-bearing potential who are unwilling to avoid pregnancy or use an effective form of birth control.
- Currently on dialysis or planning to start dialysis.
- Is currently enrolled or participated in another device, drug, or biological trial within 30 days of screening.
- Has used wound treatments with enzymes, growth factors, living skin, dermal substitutes including other amniotic or umbilical cord tissue therapies, or other advanced biological therapies within the last 30 days.
- Current use of topical anti-microbial or silver-containing products.
- Target ulcer is over an active or inactive Charcot deformity.
- The depth of the target ulcer is graded as Wagner Grade III or higher, i.e., with evidence of exposed muscle, tendon, bone, and/or joint capsule.
- Gangrene is present on any part of the affected foot.
- Current suspicion of osteomyelitis, cellulitis, or other clinical signs or symptoms of target ulcer infection.
- Any previous use of Vendaje®, Vendaje AC®, AmnioWrap2® applied to the target ulcer.
- The following additional exclusion criteria should be reviewed for all subjects at the end of the screening run-in period prior to randomization for eligibility determination:
- The target ulcer has decreased \> 30% in wound area post debridement at baseline following the two-week run-in period.
- Use of excluded concomitant medications, therapies, or procedures during the two-week run-in period.
- Has clinical signs or symptoms of infection within the target ulcer.
Key Trial Info
Start Date :
October 28 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 1 2026
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06565156
Start Date
October 28 2024
End Date
January 1 2026
Last Update
August 27 2025
Active Locations (17)
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1
Site 17
Guntersville, Alabama, United States, 35976
2
Site 22
Mesa, Arizona, United States, 85206
3
Site 25
Tucson, Arizona, United States, 85723
4
Site 19
Palmdale, California, United States, 93551