Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 4:51 PM
Ignite Modification Date:
2025-12-24 @ 4:51 PM
NCT ID:
NCT05671250
Eligibility Criteria:
Inclusion Criteria:
1. Male or female age of ≥ 18
2. Type 2 Diabetes Mellitus diagnosed as per the American Diabetic Association at the time of recruitment
3. Patients with glycated haemoglobin (HbA1C) ≤ 9% within 4 weeks prior to randomization
4. Patients with ulcer that meets the following criteria
1. Ulcers classified as Grade 1, stage A (1A) ulcers using University of Texas (UT) classification system (ulcers are superficial not involving tendon, capsule or tendon and are non-infected and non-ischemic)
2. Ulcer duration of 4 weeks or longer and hard to heal despite standard of care treatment (chronic ulcers)
3. Ulcer has undergone recent debridement (2 weeks prior to screening)
4. Post-debridement ulcer is free of necrotic debris, foreign bodies, sinus tracts, tunnelling, and undermining and is comprised of healthy vascularized tissue
5. Wound area at start of treatment between 2 sq.cm. and 10 sq.cm.
6. No surgical revascularization of the limb with the DFU was done in the previous two months.
5. Limb criteria: At least moderate blood perfusion into the affected limb as defined by Ankle Brachial Index (ABI) of 0.9 - 1.3.
6. Patients who agree to conform to the off-loading requirements
7. Provide written informed consent prior to admission into the study
Exclusion Criteria:
1. Type 1 Diabetes Mellitus
2. Patients who have undergone, in the 2-week period prior to enrolment, treatment for DFU with any advanced treatment modality other than standard of care, such as growth factors, skin substitutes or other biological treatments
3. Have a glycosylated haemoglobin (HbA1c) \> 9.0%
4. Have a body mass index (BMI) \> 40 Kg/m2
5. Have a clinically significant cardiac, gastrointestinal, endocrine, neurological, liver, or kidney disease
6. Anaemia (Haemoglobin \< 9 g/dL) or white Blood Cells count \> 11,000/μL or platelets count \< 100,000/μL or \> 400,000/μL or liver function tests \> 3 times upper normal lab values or Creatinine \> 3 mg/dL; any indication of malnourishment (Albumin \< 3 g/dL); INR \> 2 or any other clinically significant blood and urinalysis tests per the physician's discretion
7. Patients with haemochromatosis or unstable hypertension
8. Have any clinically significant chronic or acute illness during the 4 weeks prior to admission into the study, except type 2 diabetes or during screening period
9. Patients with wounds caused by basal cell carcinoma or due to basal cell carcinoma excision
10. Females who are pregnant, lactating, of child-bearing potential, or post-menopausal for less than 2 years, not using a medically approved method of contraception, or females who test positive on a blood-based pregnancy test.
11. Patients with a history of allergy to one of tested components
12. Patients on glyceryl trinitrate or Sildenafil treatment
13. Patients with a history of any clinical or laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of the investigational agent or may confound the interpretation of study results or might render the patient at high risk for treatment complications
14. Patients with active Charcot or other structural deformity that would prevent adequate off-loading of the study foot.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05671250
Study Brief:
Protocol Section:
NCT05671250