Umbilical Cord Artery-derived Perivascular Stem Cells for the Critical Limb Ischemia Therapy

NCT06174597 | Recruiting Early Phase 1 DMC

• 1 other identifier: CLI-2023
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

This clinical trial included 2 periods. During the first period, it was a single arm study to explore the safety of umbilical cord artery-derived stem cells (UCA-PSCs) in the treatment of patients with critical limb ischemia (CLI). During the second perid, it was a single-center, randomized, controlled prospective study to determine the efficacy of the UCA-PSCs treatment. Those who had CLI were enrolled in the study.

Conditions

Critical Limb Ischemia

Keywords

Critical Limb Ischemia; Umbilical cord artery-derived perivascular stem cells

Outcome Measures

Primary Outcomes (1)

• hindlimb flow index

  measured by Laser Doppler

  24 months

Secondary Outcomes (2)

• Increase in transcutaneous partial oxygen pressure (TcPO2)

  24 months

• Ankle brachial pressure index (ABPI)

  24 months

Study Arms (2)

UCA-PSCs/bFGF group

EXPERIMENTAL

Clusters of umbilical cord artery-derived perivascular stem cells (Dose: 1.2 x 10\^8 cells+20ng bFGF /20mL/vial)

Procedure: UCA-PSCs/bFGF or bFGF Intramuscular injection

bFGF group

ACTIVE COMPARATOR

(Dose: 20ng bFGF /20 mL/vial)

Procedure: UCA-PSCs/bFGF or bFGF Intramuscular injection

Interventions

UCA-PSCs/bFGF or bFGF Intramuscular injection PROCEDURE

After skin disinfection, according to the distribution characteristics of blood vessels around the vascular lesion area, the site that is most likely to establish a new collateral circulation in vascular anatomy is selected. According to the vascular lesion of each subject, 40 reasonable injection sites are selected for Clusters of umbilical cord artery-derived perivascular stem cells with bFGF or bFGF only.

UCA-PSCs/bFGF group; bFGF group

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Aged between 18 and 80, of any gender;
• Diagnosed with lower extremities ischemia, classified as Rutherford Stage IV-V, affecting at least one limb. If both lower limbs have ischemic disease, the researcher will determine which affected limb will be studied. The resting ankle systolic pressure (dorsalis pedis artery or posterior tibial artery) of the affected limb is less than 60mmHg, or the toe systolic pressure is less than 40 mmHg, or the Ankle-Brachial Index (ABI) is less than 0.50;
• Within the last month, Digital Subtraction Angiography (DSA), Computed Tomography Arteriography (CTA), Magnetic Resonance Angiography (MRA)，or vascular ultrasound has confirmed that one or more of the arteries (superficial femoral artery, i.e., the femoral artery below the deep femoral artery branch, the popliteal artery, and its following arteries) have a stenosis of ≥75% or occlusion;
• Patient experiences rest pain in the limb due to ischemia for at least two weeks;
• Inoperable or not suitable for endovascular treatment，or no obvious improvement after surgical treatment;
• Expected lifespan \>2 years;
• Good compliance, accepting dietary control and medication treatment, with an informed consent form signed by the patient themselves or their legal representatives.

You may not qualify if:

• Acute ischemic disease of the lower limb(s) occurred within the past 2 weeks, or patients with acute progression of lower extremity arterial ischemic disease, or those with local/diffuse gangrene;
• Unsatisfactory evaluation of condition stability after vascular reconstruction surgery or sympathetic nerve removal surgery performed within 4 weeks，or possibility of undergoing amputation in the next 4 weeks;
• Stenosis of ≥75% in the main-iliac artery;
• Diabetic patients with HbA1c \> 10%;
• Abnormal laboratory test results that meet any of the following criteria:i. Abnormal blood routine examination: Hemoglobin (HGB)\<80 g/L, or white blood cell count (WBC)\<3.0×10\^9/L, or platelet count (PLT)\<50×10\^9/L; ii. Abnormal liver function: Aspartate aminotransferase (AST)\>2 times the upper limit of normal (ULN), or alanine aminotransferase (ALT)\>2×ULN, total bilirubin (TBIL)\>2×ULN; iii. Severe renal dysfunction requiring dialysis treatment;iv. Other abnormal laboratory testing indicators that researchers believe may affect the evaluation of trial results;
• Diseases unsuitable for clinical trials, or contraindications to surgery: i. Difficult-to-control hypertension (\>180/110mmHg), severe heart failure (NYHA IV), or EF\<30%;ii. Patients who have had a stroke, brain hemorrhage, myocardial infarction, or unstable angina in the past one month; iii. Patients with malignant tumors;iv. Receiving immunosuppressants, hemodialysis, chemotherapy, and radiotherapy; v. Active infection, HIV antibody positive, Hepatitis C antibody positive, Hepatitis B (HBsAg positive and Hepatitis B virus DNA quantitative detection value greater than 1×10\^3 IU/mL); vi. Serious infections (like cellulitis, osteomyelitis etc.) in the observational limb, exposure of distal fascia or skeleton, unable to maintain wound care for ulcers in the surgical area etc.; vii. History of major surgery or serious injury within the last one months;
• During the trial, taking the following drugs at doses greater than stated below, except those who stop medication or adjust the dose to the prescribed dose for 7 days according to the washout period: i. COX-2 inhibitor drugs (such as nimesulide); ii. Aspirin (more than 100 mg/day);iii. High-dose steroid medications, excluding inhaled steroids; iv. Opioid analgesics (like morphine) for 2 weeks or longer;
• Congenital or acquired immunodeficiency;
• Pregnant women or those planning pregnancy;
• Diseases like pulmonary heart disease and mental illness that researchers believe are unstable and cannot complete the trial, or comorbidities that could interfere with safety checks and effectiveness assessments;
• Currently participating in other clinical trials.

Sponsors & Collaborators

• Nanjing University: lead

Study Sites (1)

The affiliated Drum Towel Hospital of Nanjing University Medical School

Nanjing, Jiangsu, 210008, China

RECRUITING

MeSH Terms

Conditions

Chronic Limb-Threatening Ischemia

Condition Hierarchy (Ancestors)

Peripheral Arterial Disease; Atherosclerosis; Arteriosclerosis; Arterial Occlusive Diseases; Vascular Diseases; Cardiovascular Diseases; Peripheral Vascular Diseases; Chronic Disease; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Ischemia

Study Officials

• Haiming Xia, phD

  The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Min Zhou, Dr.

CONTACT

13951937586; zhouminnju@126.com

Lijun Ding

CONTACT

86-25-8310-7170; xmljding@163.com

Study Design

• Study Type: interventional
• Phase: early phase 1
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: principal investigator

Study Record Dates

• First Submitted: July 19, 2023
• First Posted: December 18, 2023
• Study Start: June 30, 2023
• Primary Completion: June 30, 2024
• Study Completion: June 30, 2026
• Last Updated: December 18, 2023

Record last verified: 2023-07

Locations

CN (1)