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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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.

  1. 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.
  2. Ulcers located on the plantar, medial, or lateral aspects of the foot with a size <30 cm².
  3. 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.

Egypt1 site
  • kafr elshaikh university Hospital

    Kafrelsheikh, Kafrelsheikh, 33511

Other trials in Egypt

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.

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 groups in NCT06812637
Study groupRoleWhat they receive
Treated groupExperimental40 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 groupOther35 patients received standard of care (SOC) only for 4 weeks followed by follow-up for 16 weeks.
Placebo groupPlacebo comparator35 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.

  1. 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.

  1. First posted6 Feb 2025
  2. Study start6 Apr 2024
  3. Primary completion6 Jun 2024
  4. Study completion2 Sep 2024

Resources

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)
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

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.

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