Diabetic Foot Ulcer (DFU)Phase 1WJ-MSCNCT06812637
Efficacy and Safety of Wharton's Jelly-Derived Mesenchymal Stem Cell Exosomes in the Treatment of Diabetic Foot Ulcers: A Double-blinded Randomized Controlled Clinical Trial
A Phase 1 study testing WJ-MSC- Exosomes in people with Diabetic Foot Ulcer (DFU) and Exosomes, run by Kafrelsheikh University at 1 site in Egypt.
Trial summary
Study effeciency and safety of WJ-MSC derived exosomes in DFU healing Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Diabetic Foot Ulcer (DFU), Exosomes
- What is being tested?
- WJ-MSC- Exosomes
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 110 participants
- Where
- 1 siteEgypt
- Study dates
- 6 Apr 2024to 2 Sep 2024
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Inclusion Criteria:1. Adults aged 18 years or older with type 1 or type 2 diabetes.
- Presence of a chronic DFU persisting for more than six weeks or showing less than 30% reduction in size after a seven-day standard of care (SOC) management.
- Ulcers located on the plantar, medial, or lateral aspects of the foot with a size <30 cm².
- Patients with neuropathic, ischemic, or mixed neuropathic-ischemic ulcers. 5. Revascularization performed for ischemic ulcers before enrollment.
-
Exclusion Criteria:1. Pregnancy or breastfeeding. 2. Presence of venous ulcers or active infections. 3. Exposure of bone, ligaments, or tendons.
-
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Efficacy and Safety of Wharton's Jelly-Derived Mesenchymal Stem Cell Exosomes in the Treatment of Diabetic Foot Ulcers: A Randomized Controlled Trial
Study effeciency and safety of WJ-MSC derived exosomes in DFU healing
Read the detailed description
Diabetic foot ulcers (DFUs) represent a significant complication of diabetes mellitus, affecting a substantial proportion of patients and often leading to severe morbidity, prolonged hospital stays, and increased healthcare costs [1]. The management of DFUs remains a considerable challenge due to their chronic nature and the complex interplay of factors that impede healing, including poor blood circulation, neuropathy, and infection and this leads to the increase in the number of amputations [2].
The prevalence of diabetes mellitus (DM) is rising globally, with projections of affected individuals increasing from 463 million in 2019 to 642 million by 2040 [3], particularly in regions like the Middle East and North Africa (MENA), where Egypt ranks among the top 10 countries with the highest diabetes prevalence [4].Diabetic foot ulcers (DFUs) are a common and debilitating complication of DM, with a lifetime risk of 19-34% among diabetic patients and accounting for 85% of diabetic lower-limb amputations (DLLA) [5, 6].These ulcers significantly contribute to morbidity, prolonged hospitalizations, and a high socio-economic burden while being associated with post-amputation mortality rates of 24.6% within 5 years and 45.4% within 10 years [7].
The scale of this challenge demands urgent attention to innovative, cost-effective interventions to alleviate both human suffering and financial strain[8], various approaches have been developed to enhance healing and prevent recurrence, such as advanced wound dressings, offloading techniques, and the use of growth factors or skin substitutes [9]. But they are still far from ideal. As such, there is an urgent need for innovative therapeutic strategies that can effectively promote wound healing and improve patient outcomes. applications.
In recent years, mesenchymal stem cell (MSC) - derived exosomes have garnered attention in regenerative medicine. Exosomes are small extracellular vesicles that facilitate intercellular communication by transporting proteins, lipids, and nucleic acids. MSC-derived exosomes have demonstrated the ability to modulate inflammation, promote angiogenesis, and enhance tissue repair across various conditions, including cardiovascular diseases, osteoarthritis, and chronic wounds [10].
Traditionally, bone marrow (BM) has been the primary source of pluripotent MSCs. However, harvesting BM requires an invasive procedure, and with advancing age, the quantity, differentiation potential, and lifespan of BM-derived MSCs decline significantly So alternative sources such as the umbilical cord and adipose tissue (AD) have gained attention [11] . Among these, umbilical cord-derived MSCs, specifically those from Wharton's jelly (WJ), known as Wharton's jelly mesenchymal stem cells (WJ-MSCs) have unique properties. WJ-MSCs are highly accessible, ethically uncontroversial, and offer significant advantages, including a strong differentiation potential and an immunoprivileged status. Moreover, they exhibit characteristics similar to embryonic stem cells including rapid cell division and high expansion capacity[12].
Experimental evidence suggests that WJ-MSCs demonstrate superior proliferation potential compared other MSC such as adipose tissue-derived MSCs (AD-MSCs). These properties position WJ-MSCs as an attractive option for regenerative medicine and therapeutic applications [13, 14].
This study aims to investigate the efficacy and safety of the topical application of WJ-MSC-derived exosomes in patients with chronic DFUs, thereby exploring a potential new treatment paradigm for this debilitating condition. The outcomes of this research could not only enhance healing rates but also significantly improve the quality of life for individuals suffering from chronic diabetic foot ulcers.
- Conditions
- Diabetic Foot Ulcer (DFU), Exosomes
- Being tested
- WJ-MSC- Exosomes, SOC (Standard of care), Vehicle (placebo)
- Keywords
- Exosomes, Diabetic foot ulcer, WJ-MSC
- Medical subject headings
- Diabetic Foot
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
WJ-MSC- ExosomesDrug
warton jelly derived mesenschymal stem cell derived exosomes dissolved in CMC
SOC (Standard of care)Combination product
Wound depridement for necrotic parts , local antibiotic , dressing , unloading
Vehicle (placebo)Other
Vehicle for the MSC-EXO
| Study group | Role | What they receive |
|---|---|---|
| Treated group | Experimental | 40 patients received standard of care (SOC) with Wharton jelly derived mesenchymal stem cell (WJ - MSC) exosome gel once weekly for 4 weeks followed by follow up for 16 weeks Receives: Drug: WJ-MSC- Exosomes; Combination Product: SOC (Standard of care) |
| Control group | Other | 35 patients received standard of care (SOC) only for 4 weeks followed by follow-up for 16 weeks. |
| Placebo group | Placebo comparator | 35 patients received received a visually identical saline-based formulation once weekly for 4 weeks followed by follow up for 16 weeks together with SOC |
What is being measured
The primary outcome is the main question the study is designed to answer.
Ulcer healing
measuring the percent of wound closure compared to the baseline
Measured: 20 week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Feb 2025
- Study start6 Apr 2024
- Primary completion6 Jun 2024
- Study completion2 Sep 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Diabetic Foot Ulcer (DFU)Studies of the same condition, open and under way.
- More trials run by Kafrelsheikh UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This was a prospective, randomized, double-blind, placebo-controlled clinical trial conducted to evaluate the efficacy and safety of WJ-MSC-derived exosomes gel in patients with diabetic foot ulcers (DFUs).
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Outcomes assessor
- Enrolment
- 110 participants (actual)
Sponsor and investigators
- Lead sponsor
- Kafrelsheikh University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Abdallah Mohammed Hafez, Kafrelsheikh University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06812637
- Sponsor's protocol ID
- WJ-MSC-exo in diabetic foot
- Acronym
- WJ-MSC
- Status last verified
- Feb 2025
- First submitted
- 2 Feb 2025
- Last updated
- 29 Apr 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: iam not sure i will share patient private data untill i have aprovement from them
Study at a glance
From the registry record, last updated by the sponsor on 29 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy and Safety of Wharton's Jelly-Derived Mesenchymal Stem Cell Exosomes in the Treatment of Diabetic Foot Ulcers: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT06812637
- Acronym / sponsor ID
- WJ-MSC / WJ-MSC-exo in diabetic foot
- Conditions
- Diabetic Foot Ulcer (DFU), Exosomes
- Keywords
- Exosomes, Diabetic foot ulcer, WJ-MSC
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 110 participants (actual)
- Lead sponsor
- Kafrelsheikh UniversityUniversity, hospital or other
- Study start
- 6 Apr 2024 (actual)
- Primary completion
- 6 Jun 2024 (actual)
- Study completion
- 2 Sep 2024 (actual)
- First posted
- 6 Feb 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Study effeciency and safety of WJ-MSC derived exosomes in DFU healing
Detailed description
Diabetic foot ulcers (DFUs) represent a significant complication of diabetes mellitus, affecting a substantial proportion of patients and often leading to severe morbidity, prolonged hospital stays, and increased healthcare costs [1]. The management of DFUs remains a considerable challenge due to their chronic nature and the complex interplay of factors that impede healing, including poor blood circulation, neuropathy, and infection and this leads to the increase in the number of amputations [2].
The prevalence of diabetes mellitus (DM) is rising globally, with projections of affected individuals increasing from 463 million in 2019 to 642 million by 2040 [3], particularly in regions like the Middle East and North Africa (MENA), where Egypt ranks among the top 10 countries with the highest diabetes prevalence [4].Diabetic foot ulcers (DFUs) are a common and debilitating complication of DM, with a lifetime risk of 19-34% among diabetic patients and accounting for 85% of diabetic lower-limb amputations (DLLA) [5, 6].These ulcers significantly contribute to morbidity, prolonged hospitalizations, and a high socio-economic burden while being associated with post-amputation mortality rates of 24.6% within 5 years and 45.4% within 10 years [7].
The scale of this challenge demands urgent attention to innovative, cost-effective interventions to alleviate both human suffering and financial strain[8], various approaches have been developed to enhance healing and prevent recurrence, such as advanced wound dressings, offloading techniques, and the use of growth factors or skin substitutes [9]. But they are still far from ideal. As such, there is an urgent need for innovative therapeutic strategies that can effectively promote wound healing and improve patient outcomes. applications.
In recent years, mesenchymal stem cell (MSC) - derived exosomes have garnered attention in regenerative medicine. Exosomes are small extracellular vesicles that facilitate intercellular communication by transporting proteins, lipids, and nucleic acids. MSC-derived exosomes have demonstrated the ability to modulate inflammation, promote angiogenesis, and enhance tissue repair across various conditions, including cardiovascular diseases, osteoarthritis, and chronic wounds [10].
Traditionally, bone marrow (BM) has been the primary source of pluripotent MSCs. However, harvesting BM requires an invasive procedure, and with advancing age, the quantity, differentiation potential, and lifespan of BM-derived MSCs decline significantly So alternative sources such as the umbilical cord and adipose tissue (AD) have gained attention [11] . Among these, umbilical cord-derived MSCs, specifically those from Wharton's jelly (WJ), known as Wharton's jelly mesenchymal stem cells (WJ-MSCs) have unique properties. WJ-MSCs are highly accessible, ethically uncontroversial, and offer significant advantages, including a strong differentiation potential and an immunoprivileged status. Moreover, they exhibit characteristics similar to embryonic stem cells including rapid cell division and high expansion capacity[12].
Experimental evidence suggests that WJ-MSCs demonstrate superior proliferation potential compared other MSC such as adipose tissue-derived MSCs (AD-MSCs). These properties position WJ-MSCs as an attractive option for regenerative medicine and therapeutic applications [13, 14].
This study aims to investigate the efficacy and safety of the topical application of WJ-MSC-derived exosomes in patients with chronic DFUs, thereby exploring a potential new treatment paradigm for this debilitating condition. The outcomes of this research could not only enhance healing rates but also significantly improve the quality of life for individuals suffering from chronic diabetic foot ulcers.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, outcomes assessor)
- Number of arms
- 3
- Model description
- This was a prospective, randomized, double-blind, placebo-controlled clinical trial conducted to evaluate the efficacy and safety of WJ-MSC-derived exosomes gel in patients with diabetic foot ulcers (DFUs).
| Arm | Type | Receives |
|---|---|---|
| Treated group | Experimental | Drug: WJ-MSC- Exosomes, Combination Product: SOC (Standard of care)40 patients received standard of care (SOC) with Wharton jelly derived mesenchymal stem cell (WJ - MSC) exosome gel once weekly for 4 weeks followed by follow up for 16 weeks |
| Control group | Other | –35 patients received standard of care (SOC) only for 4 weeks followed by follow-up for 16 weeks. |
| Placebo group | Placebo comparator | –35 patients received received a visually identical saline-based formulation once weekly for 4 weeks followed by follow up for 16 weeks together with SOC |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| WJ-MSC- Exosomeswarton jelly derived mesenschymal stem cell derived exosomes dissolved in CMC | Drug | Treated group |
| SOC (Standard of care)Wound depridement for necrotic parts , local antibiotic , dressing , unloading | Combination product | Treated group |
| Vehicle (placebo)Vehicle for the MSC-EXO | Other | – |
Primary outcome
Ulcer healing
Time frame: 20 week
measuring the percent of wound closure compared to the baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Apr 2025.
- Individual participant dataSharing planned: Undecided. iam not sure i will share patient private data untill i have aprovement from them
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing WJ-MSC- Exosomes in people with Diabetic Foot Ulcer (DFU) and Exosomes, run by Kafrelsheikh University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 29 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Ulcer healing (time frame: 20 week). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Apr 2025.