Skip to main content
Clinical Trials/NCT02915796
NCT02915796
Unknown
Phase 1

Autologous CD133(+) Cells as an Adjuvant to Below the Knee Percutaneous Transluminal Angioplasty: A Randomized Controlled Clinical Trial in Diabetic Patients With Below the Knee Critical Limb Ischemia

Shanghai 10th People's Hospital1 site in 1 country345 target enrollmentSeptember 2016

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Peripheral Arterial Disease
Sponsor
Shanghai 10th People's Hospital
Enrollment
345
Locations
1
Primary Endpoint
Restenosis rate
Last Updated
9 years ago

Overview

Brief Summary

The main aim of the present study was to evaluate the therapeutic potential and safety of transarterial infusion of granulocyte colony stimulating factor (G-CSF) mobilized cluster of differentiation (CD) 133(+) cells when combined with percutaneous transluminal angioplasty (PTA) in treatment of below the knee (BTK) peripheral arterial disease (PAD) in diabetic patients.

Detailed Description

CD133+ cell, a bone marrow derived subpopulation of adult hematopoietic progenitor cells, confers high proliferative, vasculogenic and regenerative capacity in vitro and in vivo. thereby suggesting that CD133+ cells may induce vasculogenesis, improve limb perfusion, prevent tissue loss and restore ambulatory function in patients with critical limb ischemia. Although several small, randomized trials have been conducted so far demonstrating safety of autologous cells of bone marrow origin for the treatment, the reported benefits were found to be variable. A meta-analysis of autologous bone marrow derived cell therapy for critical limb ischemia trials suggested that application of autologous stem cell transplantation in curing limb ischemic patients does not have obviously effectiveness in the improvement of ankle brachial pressure (ABI) of the limb ischemic patients. But it can dramatically reduce the rate of amputation. Therefore, in the present study, the investigators aim to evaluate the therapeutic potential and safety of transarterial infusion of g-csf-mobilized CD 133(+) cells when combined with PTA in treatment of below the knee PAD in diabetic patients.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
April 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shanghai 10th People's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Maoquan Li

Prof. Dr. Li

Shanghai 10th People's Hospital

Eligibility Criteria

Inclusion Criteria

  • Age range: 18-75 years , Gender: Both
  • Patients with below the knee limb ischemia with diabetes.
  • Rutherford class 2-
  • Target lesions with a diameter reduction of at least 50% and have an occlusion of longer than 4 cm on angiography.
  • Have no previous history of any stem cell therapy \[infusion of CD133 endothelial progenitor cell (EPC)\].
  • Written informed consent signed by the patients or representatives. -

Exclusion Criteria

  • Previous bypass surgery or stent placement at the ipsilateral lower limb
  • History of intolerance to antiplatelet therapy, heparin, or contrast media.
  • Presence of any of the following conditions:
  • severe liver disease (such as ascites, esophageal varices, liver transplantation);
  • hemodynamic instability;
  • Severely impaired renal function (serum creatinine level \> 2.5 mg/dL).
  • Receiving immunosuppressive therapy;
  • History of decompensated heart failure (New York Heart Association class III or IV and level) or myocardial infarction, or heart bypass surgery;
  • Bleeding diathesis;
  • Active systemic bacterial infection;

Outcomes

Primary Outcomes

Restenosis rate

Time Frame: 12 months

Occurrence of \> 50% of restenosis in the treated vessel after 12 months as assessed by digital substraction angiography (DSA) (Efficacy endpoints).

Peak systolic velocity ratio

Time Frame: 12 months

Peak systolic velocity ratio ≥ 2.4 by Doppler's ultrasonography for patients who did not undergo angiography after 12 months (Efficacy endpoints).

Severe adverse effects (SAEs)

Time Frame: 12 months

Number of SAEs per subject across actual treatment cohorts (Safety Endpoint).

Secondary Outcomes

  • ABI value(6 and 12 months)
  • Transcutaneous oxygen pressures (TcPO2)(6 and 12 months)
  • Amputation-free survival (AFS)(6 and 12 months)
  • Rutherford classification(6 and 12 months)
  • Rest pain(6 and 12 months)
  • Six Minute Walk test(6 and 12 months)
  • Ulcer healing rate(6 and 12 months)

Study Sites (1)

Loading locations...

Similar Trials