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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

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

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

Intervensjonell

Registrering (Faktiske)

15

Fase

  • Fase 2
  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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,…)

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Andre navn:
  • Implant of ASCs.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Security and tolerance
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
therapeutic effect
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studieleder: Felipe Prosper, MD, PhD, Clinica Universidad De Navarra

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. juni 2010

Primær fullføring (Faktiske)

1. september 2013

Studiet fullført (Faktiske)

1. september 2013

Datoer for studieregistrering

Først innsendt

5. juli 2010

Først innsendt som oppfylte QC-kriteriene

6. juli 2010

Først lagt ut (Anslag)

7. juli 2010

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

8. november 2016

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. november 2016

Sist bekreftet

1. november 2016

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

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

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Kliniske studier på Crohns sykdom

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