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Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI) (JUVENTAS)

Primary Purpose

Peripheral Vascular Diseases, Arterial Occlusive Diseases, Leg Ulcer

Status
Completed
Phase
Phase 1
Locations
Netherlands
Study Type
Interventional
Intervention
Bone marrow punction
BM-MNC infusion
Placebo infusion
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Vascular Diseases focused on measuring clinical trial, chronic critical limb ischemia, leg pain, cell therapy, bone marrow, mononuclear, progenitor cell, stem cell, critical limb ischemia, nonhealing leg ulcer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18 years
  • Severe infra-popliteal peripheral arterial occlusive disease [PAOD] (Fontaine class IIb, III or IV)
  • Invalidating intermittent claudication, persistent, recurring rest pain requiring analgesia and/or non-healing ulcers present for > 4 weeks without evidence of improvement in response to conventional therapies
  • Ankle brachial index < 0.6 or "unreliable"
  • Not eligible for surgical or radiological revascularization
  • Written informed consent

Exclusion Criteria:

  • History of neoplasm or malignancy in the past 10 years
  • Serious known concomitant disease with life expectancy of less than one year
  • Anticipated inability to obtain 100 ml of bone marrow aspirate
  • Known infection with human immunodeficiency virus (HIV), hepatitis B or hepatitis C virus
  • Follow-up impossible

Sites / Locations

  • University Medical Center Utrecht (UMC Utrecht)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

BM-MNC

Placebo

Arm Description

autologous bone marrow-derived mononuclear cells

Placebo

Outcomes

Primary Outcome Measures

major amputation

Secondary Outcome Measures

minor amputation
number and extent of leg ulcers
resolvement of rest pain
improvement of ankle-brachial index (ABI)
improvement transcutaneous oxygen pressure (TcpO2)
changes in quality of life
changes in clinical status (Rutherford classification)

Full Information

First Posted
September 1, 2006
Last Updated
December 12, 2012
Sponsor
UMC Utrecht
Collaborators
Catharijne Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00371371
Brief Title
Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI)
Acronym
JUVENTAS
Official Title
Intra-arterial Infusion of Autologous Bone Marrow Mononuclear Cells in Patients With Chronic Critical Limb Ischemia: a Randomized, Placebo-controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht
Collaborators
Catharijne Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purposes of this study are to determine whether intra-arterial injection of autologous stem cells is effective in the treatment of chronic limb ischemia (CLI), to characterize stem cell dysfunction in patients with CLI, and to relate the stem cell function with clinical outcome.
Detailed Description
Despite advances in surgical and radiological vascular techniques, a significant number of patients with chronic critical limb ischaemia (CLI) are not eligible for revascularization procedures, often leaving amputation as the only option. Consequently, exploring new strategies for revascularization of ischemic limbs is of major importance. Preclinical studies and pioneering clinical trials suggest that administration of bone marrow (BM) mononuclear cells (MNC) into ischemic limbs enhances neovascularization, improves tissue perfusion and prevents amputation. However, no definite proof is available as the clinical studies thus far have been small and lacked double-blinded controls. JUVENTAS is a randomized, double-blinded placebo-controlled trial in 109 - 160 patients with CLI to investigate the potential clinical effects of repeated intra-arterial infusion of BM-MNC in these patients (the exact number of patients to be included cannot be specified in advance because of the planned group sequential interim analyses). In addition, it will study the functional characteristics of the BM-MNC obtained from CLI patients and relate BM-MNC dysfunction to clinical outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Vascular Diseases, Arterial Occlusive Diseases, Leg Ulcer, Gangrene, Ischemia
Keywords
clinical trial, chronic critical limb ischemia, leg pain, cell therapy, bone marrow, mononuclear, progenitor cell, stem cell, critical limb ischemia, nonhealing leg ulcer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
160 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BM-MNC
Arm Type
Experimental
Arm Description
autologous bone marrow-derived mononuclear cells
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Procedure
Intervention Name(s)
Bone marrow punction
Intervention Description
A total volume of 100 ml bone marrow will be aspirated from the iliac crest under local anaesthesia (lidocaine) according to local routine. To maximise the patients comfort, 5-10 mg midazolam and 50 ug fentanyl will be administered intravenously.
Intervention Type
Procedure
Intervention Name(s)
BM-MNC infusion
Intervention Description
Repeated intra-arterial infusion of autologous BM-MNC into the common femoral artery
Intervention Type
Procedure
Intervention Name(s)
Placebo infusion
Intervention Description
Repeated intra-arterial infusion of placebo (PBS/4% HAS/heparin, coloured with autologous erythrocytes to match the colour of BM-MNC suspension) into the common femoral artery.
Primary Outcome Measure Information:
Title
major amputation
Time Frame
six months
Secondary Outcome Measure Information:
Title
minor amputation
Time Frame
six months
Title
number and extent of leg ulcers
Time Frame
six months
Title
resolvement of rest pain
Time Frame
six months
Title
improvement of ankle-brachial index (ABI)
Time Frame
six months
Title
improvement transcutaneous oxygen pressure (TcpO2)
Time Frame
six months
Title
changes in quality of life
Time Frame
suix months
Title
changes in clinical status (Rutherford classification)
Time Frame
six months
Other Pre-specified Outcome Measures:
Title
Amputation-free survival
Time Frame
six months
Title
Treatment failure
Description
Composite endpoint defined as major amputation of treated leg, all-cause mortality, doubling in total wound surface area, or de novo gangrene
Time Frame
six months
Title
Successfull treatment
Description
Composite endpoint defined as subject is (A) alive, (B) without major amputation of index limb, (C) not worsened rutherford class or VAS, and (D) improved in either Rutherford or VAS (>30mm)
Time Frame
six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years Severe infra-popliteal peripheral arterial occlusive disease [PAOD] (Fontaine class IIb, III or IV) Invalidating intermittent claudication, persistent, recurring rest pain requiring analgesia and/or non-healing ulcers present for > 4 weeks without evidence of improvement in response to conventional therapies Ankle brachial index < 0.6 or "unreliable" Not eligible for surgical or radiological revascularization Written informed consent Exclusion Criteria: History of neoplasm or malignancy in the past 10 years Serious known concomitant disease with life expectancy of less than one year Anticipated inability to obtain 100 ml of bone marrow aspirate Known infection with human immunodeficiency virus (HIV), hepatitis B or hepatitis C virus Follow-up impossible
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frans L Moll, MD, PhD
Organizational Affiliation
UMC Utrecht
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Marianne C Verhaar, MD, PhD
Organizational Affiliation
UMC Utrecht
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ralf W Sprengers, MD, PhD
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martin Teraa, MD
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Utrecht (UMC Utrecht)
City
Utrecht
ZIP/Postal Code
3508 GA
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
18376183
Citation
Sprengers RW, Lips DJ, Moll FL, Verhaar MC. Progenitor cell therapy in patients with critical limb ischemia without surgical options. Ann Surg. 2008 Mar;247(3):411-20. doi: 10.1097/SLA.0b013e318153fdcb.
Results Reference
background
PubMed Identifier
19837547
Citation
Sprengers RW, Janssen KJ, Moll FL, Verhaar MC, van der Graaf Y; SMART Study Group. Prediction rule for cardiovascular events and mortality in peripheral arterial disease patients: data from the prospective Second Manifestations of ARTerial disease (SMART) cohort study. J Vasc Surg. 2009 Dec;50(6):1369-76. doi: 10.1016/j.jvs.2009.07.095. Epub 2009 Oct 17.
Results Reference
background
PubMed Identifier
20153223
Citation
Sprengers RW, Moll FL, Verhaar MC. Stem cell therapy in PAD. Eur J Vasc Endovasc Surg. 2010 Mar;39 Suppl 1:S38-43. doi: 10.1016/j.ejvs.2009.12.001. Epub 2010 Feb 12.
Results Reference
background
PubMed Identifier
20488328
Citation
Sprengers RW, Moll FL, Teraa M, Verhaar MC; JUVENTAS Study Group. Rationale and design of the JUVENTAS trial for repeated intra-arterial infusion of autologous bone marrow-derived mononuclear cells in patients with critical limb ischemia. J Vasc Surg. 2010 Jun;51(6):1564-8. doi: 10.1016/j.jvs.2010.02.020.
Results Reference
background
PubMed Identifier
20598482
Citation
Sprengers RW, Teraa M, Moll FL, de Wit GA, van der Graaf Y, Verhaar MC; JUVENTAS Study Group; SMART Study Group. Quality of life in patients with no-option critical limb ischemia underlines the need for new effective treatment. J Vasc Surg. 2010 Oct;52(4):843-9, 849.e1. doi: 10.1016/j.jvs.2010.04.057.
Results Reference
background
PubMed Identifier
35802393
Citation
Moazzami B, Mohammadpour Z, Zabala ZE, Farokhi E, Roohi A, Dolmatova E, Moazzami K. Local intramuscular transplantation of autologous bone marrow mononuclear cells for critical lower limb ischaemia. Cochrane Database Syst Rev. 2022 Jul 8;7(7):CD008347. doi: 10.1002/14651858.CD008347.pub4.
Results Reference
derived
PubMed Identifier
33144352
Citation
Hanssen NMJ, Teraa M, Scheijen JLJM, Van de Waarenburg M, Gremmels H, Stehouwer CDA, Verhaar MC, Schalkwijk CG. Plasma Methylglyoxal Levels Are Associated With Amputations and Mortality in Severe Limb Ischemia Patients With and Without Diabetes. Diabetes Care. 2021 Jan;44(1):157-163. doi: 10.2337/dc20-0581. Epub 2020 Nov 3.
Results Reference
derived
PubMed Identifier
26428987
Citation
Teraa M, Schutgens RE, Sprengers RW, Slaper-Cortenbach I, Moll FL, Verhaar MC; Juventas Study Group. Core diameter of bone marrow aspiration devices influences cell density of bone marrow aspirate in patients with severe peripheral artery disease. Cytotherapy. 2015 Dec;17(12):1807-12. doi: 10.1016/j.jcyt.2015.08.004. Epub 2015 Sep 28.
Results Reference
derived
PubMed Identifier
26148006
Citation
Wisman PP, Teraa M, de Borst GJ, Verhaar MC, Roest M, Moll FL. Baseline Platelet Activation and Reactivity in Patients with Critical Limb Ischemia. PLoS One. 2015 Jul 6;10(7):e0131356. doi: 10.1371/journal.pone.0131356. eCollection 2015.
Results Reference
derived
PubMed Identifier
25567765
Citation
Teraa M, Sprengers RW, Schutgens RE, Slaper-Cortenbach IC, van der Graaf Y, Algra A, van der Tweel I, Doevendans PA, Mali WP, Moll FL, Verhaar MC. Effect of repetitive intra-arterial infusion of bone marrow mononuclear cells in patients with no-option limb ischemia: the randomized, double-blind, placebo-controlled Rejuvenating Endothelial Progenitor Cells via Transcutaneous Intra-arterial Supplementation (JUVENTAS) trial. Circulation. 2015 Mar 10;131(10):851-60. doi: 10.1161/CIRCULATIONAHA.114.012913. Epub 2015 Jan 7.
Results Reference
derived
PubMed Identifier
24218170
Citation
Teraa M, Fledderus JO, Rozbeh RI, Leguit RJ, Verhaar MC; Juventas Study Groupdagger. Bone marrow microvascular and neuropathic alterations in patients with critical limb ischemia. Circ Res. 2014 Jan 17;114(2):311-4. doi: 10.1161/CIRCRESAHA.114.302791. Epub 2013 Nov 11.
Results Reference
derived

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Intra-arterial Stem Cell Therapy for Patients With Chronic Limb Ischemia (CLI)

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