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Treatment of Fistulous Crohn's Disease by Implant of Autologous Mesenchymal Stem Cells Derived From Adipose Tissue

Primary outcome measure:

Evaluation of viability, security and tolerance of the adipose-derived mesenchymal stem cells implant (ASCs) in fistulizing Crohn's disease patients, collecting the reactions and adverse events occurred during the study.

Secondary outcome measures:

  1. Evaluating the Adipose-derived mesenchymal stem cells therapeutic effect, in particular:

    • Fistulas healing efficiency
    • Changes in quality of life in patients treated
    • Changes of systemic Crohn's disease after implant
    • Relapse rate monitored among patients who achieved Adipose-derived mesenchymal Stem Cells treatment success.
  2. Achieving the biological characterization of the cell product used and its correlation with the therapeutic effect measured with:

    • Phenotype study
    • Suppressor capacity study.
    • Citoquines production analysis

Studie Overzicht

Toestand

Voltooid

Conditie

Gedetailleerde beschrijving

The aim of this study is to evaluate the role of Autologous Mesechymal Stem Cells derived from adipose tissue in the treatment of fistulous Crohn disease.

15 Crohn's disease patients with one or more enterocutaneous, recto-vaginal or complex perianal fistula, will be included.

The trial is divided in three phases:

I. - Selection: Patients evaluation for study eligibility will take place within two weeks after Informed Consent signature.

Fistulous disease will be evaluated by MRI for perianal and rectovaginal fistulas, and by CT scan in the case of enterocutaneous fistula.

Previous laboratory test and radiological studies are valid for evaluation if they were obtained within two and six months, respectively, prior to this evaluation, and in the absence of clinical changes.

II.- Treatment phase includes:

  1. Liposuction procedure to obtain adipose tissue.
  2. Processing and production of Autologous Mesenchymal Stem Cells from adipose tissue (ASCs)
  3. ASCs implant

III.- Follow up: Study visits post-implant will take place at the 1st week (+/- 3 days), 4th week (+/- 3 days), 8th week (+/- 7 days), 12nd week (+/- 7 days), 24th week (+/- 7 days), and 1 year (+/- 7 days) after implant.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

15

Fase

  • Fase 2
  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

      • Pamplona, Spanje, 31008
        • Clinica Universitaria de Navarra
      • Pamplona, Spanje, 31008
        • Hospital Virgen del Camino
      • Pamplona, Spanje, 31008
        • Hospital Provincial de Navarra

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  1. Fistulizing Crohn´s disease patients with 1 or more enterocutaneous fistulas, recto-vaginal fistula or complex perianal fistula. The complex perianal fistula is defined as a fistula presenting one of these conditions:

    • Trans-sphincteric, supra-sphincteric or extra-sphincteric tract, determined with:
    • Clinical criteria: No palpation of the tract and surgical exploration
    • Radiological criteria: Nucleal Magnetic Resonance (NMR)or Echoendoscopy
    • Multiple fistulas
    • "Horseshoe" fistula
    • Any fistula with fecal incontinence associated
    • Any fistula with a risk of fecal incontinence as a result of:
    • previous anal fistula surgery or other perianal pathology (hemorrhoids, fissures), that involves lesions or muscular complications.
    • Obstetric or iatrogenic sphincter lesions
  2. Patients with Crohn Disease (CD) at screening and been diagnosed within 12 months before acceptance of clinical, endoscopical, anatomopathological and/or radiological criteria and have a non-active CD.(Crohn´s Disease Activity Index (CDAI)≤ 200)
  3. > 18 Years and both genders eligible.
  4. Negative pregnancy test In female fertile subjects
  5. Patient must voluntary sign the informed consent before performance of any study-related procedure not part of normal medical care.
  6. Patient is, in the investigator's opinion, willing and able to comply with the protocol requirements

Exclusion Criteria:

  1. Patients with a highly active CD, i.e., if they meet any of the following criteria:

    • Presence of severe proctitis (prominent friability, spontaneous bleeding, multiple erosions, deep ulcers) or dominant active luminal disease that requires immediate treatment, revealed by rectosigmoidoscopy
    • CDAI ≥201
  2. Presence of abscess or other collections not drained (revealed by basal radiologic study).
  3. Presence of setons drainage, unless they are removed before treatment beginning.
  4. Rectal and/ or anal stenosis revealed with rectoscopy or EBA.
  5. Patients needs surgery in the perianal region for other reasons than fistulas at inclusion or within 26 weeks after treatment administration.
  6. Patients who have received infliximab or any other anti-TNF agent within 8 weeks before the cell treatment administration.
  7. Patients who have received tacrolimus or cyclosporine within 4 weeks before cell treatment.
  8. Patients with a history of alcohol or other addictive substances abuse within 6 months before inclusion.
  9. Severe uncontrolled diseases (chronic renal failure, cardio, pulmonary,…).
  10. Any type of medical or psychiatric disease which are considered as exclusion criteria, in the investigator's opinion.
  11. Patients with diagnosis of malignant neoplasia, except basal cell or epidermoid carcinoma of the skin or previous history of malignant tumours, except those that have no evidence of relapse for at least 5 years.
  12. Subjects with congenital or acquired immunodeficiency.
  13. Positive serology for Human Immunodeficiency Virus (HIV), Hepatitis B Virus (HBV) or Hepatitis C Virus (HCV).
  14. Patient had major surgery or serious traumatism within 6 weeks before enrolment.
  15. Pregnant or breast-feeding women.
  16. Physical or psychical impossibility of following the protocol requirements
  17. Patients who are receiving or received other investigational drugs within 30 days prior to basal visit.
  18. Impossibility of doing an radiological exploration (reaction to contrast material, pacemakers, claustrophobia,…)

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Autologous mesenchymal stem cells
Fistulizing Crohn's disease

The trial is divided in three phases:

I. - Selection: Patients evaluation for study eligibility will take place within two weeks after Informed Consent signature.

II.- Treatment phase includes:

  1. Liposuction procedure to obtain adipose tissue.
  2. Processing and production of Autologous Mesenchymal Stem Cells from adipose tissue (ASCs)
  3. ASCs implant

III.- Follow up: Study visits post-implant will take place at the 1st week (+/- 3 days), 4th week (+/- 3 days), 8th week (+/- 7 days), 12nd week (+/- 7 days), 24th week (+/- 7 days), and 1 year (+/- 7 days) after implant.

Andere namen:
  • Implant of ASCs.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Security and tolerance
Tijdsspanne: 3 years
Evaluation of viability, security and tolerance of the adipose-derived mesenchymal stem cells implant (ASCs) in fistulizing Chron's disease patients, collecting the reactions and adverse events occurred during the study
3 years

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
therapeutic effect
Tijdsspanne: 3 years
  1. Evaluting the ASCs therapeutic effect, in particular:

    • Fistulas healing efficiency
    • Changes in quality of life in patients treated
    • Changes of systemic Crohn's disease after implant
    • Relapse rate monitored among patients who achieved ASCs treatment success.
  2. Achieving the biological characterization of the cell product used and its correlation with the therapeutic effect measured with:

    • Phenotype study
    • Suppressor capacity study.
    • Citoquines production analysis
3 years

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Studie directeur: Felipe Prosper, MD, PhD, Clinica Universidad de Navarra

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 juni 2010

Primaire voltooiing (Werkelijk)

1 september 2013

Studie voltooiing (Werkelijk)

1 september 2013

Studieregistratiedata

Eerst ingediend

5 juli 2010

Eerst ingediend dat voldeed aan de QC-criteria

6 juli 2010

Eerst geplaatst (Schatting)

7 juli 2010

Updates van studierecords

Laatste update geplaatst (Schatting)

8 november 2016

Laatste update ingediend die voldeed aan QC-criteria

7 november 2016

Laatst geverifieerd

1 november 2016

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • CSM/CROH
  • 2009-009880-71 (EudraCT-nummer)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

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