Umbilical cord stem cells injected into legs to fight diabetic nerve pain
NCT ID NCT07183761
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether injecting stem cells from umbilical cords into the legs can help people with moderate to severe diabetic nerve damage. 140 adults will get either stem cell shots plus standard care, or standard care alone, and be followed for 24 weeks. The goal is to see if the treatment improves nerve function and reduces pain safely.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- human umbilical cord mesenchymal stem cells (hUC-MSCs)
- What this could lead to
- If it works, this could point toward a new treatment that reduces nerve pain and improves function in people with diabetic nerve damage.
- What could go wrong
- This is an early Phase 2 trial with only 140 people, so results may not apply to everyone. Stem cell therapies can have side effects like injection site reactions or immune responses.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 140 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Males or females aged 18-80 years; 2. Meeting the 2023 ADA diagnostic criteria for type 2 diabetes; 3. Presence of symptoms and signs of diabetic neuropathy in lower extremities: For symptomatic patients: At least one abnormal finding among ankle reflex, pinprick sensation, vibration sense, pressure perception, or temperature sensation, accompanied by clinical symptoms (e.g., symmetric lower limb numbness, pain, or tingling); For asymptomatic patients: At least two abnormal findings in the above five examinations; 4. Confirmed neurophysiological dysfunction: Reduced nerve conduction velocity (≥2 standard deviations) in at least one lower extremity nerve (common peroneal, posterior tibial, or deep peroneal nerve), with or without decreased amplitude; Moderate to severe neuropathy severity: 5. Toronto Clinical Scoring System (TCSS) score ≥9; 6. Inadequate response to conventional therapy: Persistent symptoms (reduction of TCSS score \<2 points from baseline) despite ≥3 months of conventinal treatment; 7. Capacity to understand and voluntarily complete all study procedures and interventions, with signed informed consent. Exclusion Criteria: 1. Non-diabetic neuropathy or pain conditions in lower limbs that may confound DPN assessment per investigator's judgment; 2. Poorly controlled diabetes (HbA1c \>12%); 3. Severe hematological, hepatic, or renal dysfunction, meeting any of the following laboratory criteria: Hematology: Neutrophils \<1.5×10⁹/L, platelets \<90×10⁹/L, or hemoglobin \<80 g/L; Liver function: ALT or AST \>3× upper limit of normal (ULN), or total bilirubin \>1.5× ULN; Renal function: eGFR \<30 mL/min/1.73m² (calculated by MDRD formula) or requiring renal replacement therapy; Creatine kinase \>2× ULN; 4. Known allergy to stem cells, stem cell-derived products, or components of stem cell preparations; 5. Current use of prohibited medications within 5 half-lives prior to enrollment (may be reconsidered after ≥5 half-lives washout); 6. Uncontrolled systemic diseases, including but not limited to: Severe uncontrolled systemic infections (bacterial, fungal, or viral); Severe autoimmune disorders; Hematological diseases; Heart failure (NYHA class ≥III); 7. Clinically significant arrhythmia on 12-lead ECG; 8. Conditions requiring amputation (e.g., severe diabetic foot or lower limb ulcers) that preclude local stem cell injection; 9. Other diseases unsuitable for trial participation (e.g., active malignancy, cognitive impairment, depression, or psychiatric disorders); 10. Participation in any interventional clinical trial within 3 months prior to screening; 11. Pregnancy, lactation, or planning pregnancy within 2 years; 12. Any other condition deemed by the investigator to compromise trial suitability.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Southwest Hospital
RECRUITINGChongqing, Chongqing Municipality, 400038, China
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- Ancient herbal remedy put to the test against Diabetes' nerve damage
- A new pill takes aim at diabetic nerve pain — will it work?
- A ZAP BEHIND THE KNEE MAY QUIET DIABETIC NERVE PAIN