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NCT Number: NCT06303752

Tissue Therapy of Transsphincteric Anal Fistula

This clinical study aims to evaluate the outcome of the treatment of complex perianal fistulas (PAF) by the combination of minimal surgical debridement with regenerative cellular therapeutics.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

About this study

After being informed about the study and potential risks, all patients giving written informed consent will undergo screening serology and preoperative work-up to determine eligibility for study entery. Patients who meet the eligibility requirements will be treated for their fistulas by combined minor surgical debridement of the fistula tract and closure of the internal orifice as well as liposuction from the abdominal wall. Regenerative cells- enriched lipoaspirate will be injected around the entire length of the fistula tract. The first five patients will receive their own regenerative cells and act as donors for the next included patients, but they will not be included in the final analysis. The rest of the included patients (70) will be randomized in double-blinded manner (participant and investigator) in a 1:1 ratio to either recieve own regenerative cells (ADRC Adipose-Derived Regeneative Cells) or donated cultured regenerative cells (ADRC001). All included patients will be scheduled for follow-up at 3, 6 and 12 months after treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criterion:

Adult patients (>= 18years) with complex anal fistula (high transsphincteric or suprasphincteric), with involvement of more 30% of the anal sphincter referred to the surgical department at Odense University Hospital for treatment, and who are:

  • able to communicate with Danish language
  • able to provide informed consent
  • having address in the region of southern Denmark during the study

Exclusion criteria

  • Signs of suppuration/cavitation around the fistula
  • Simple or low anal fistula, which can be treated by simple surgical incision
  • Ano-vaginal and recto-vaginal fistula
  • The presence of more than one fistula tract, more than two external orifices or more than one internal orifice
  • Inflammatory Bowel Disease
  • Immunosuppression (due to clinical condition or medical therapy)
  • Malignancy within 5 years
  • Previous radiotherapy of the abdomen and pelvis
  • BMI under 18.5
  • Allergy against the antibiotics: Penicillin and streptomycin.
  • Coagulopathy
  • Pregnancy and lactation (positive HCG (human chorionic gonadotropin) test)
  • Verified syphilis, HIV, or hepatitis on screening test

Treatment and study plan

ADRC injection

Drug

Allocated patients will receive injection of 5 ml suspension including 30 million autologous adipose-derived regenerative cells ADRC and injected at the same site of the lipoaspirate injection.

Other names: Liposuction, Surgical debridement of fistula tract and closure of internal orifice, Injection of lipoaspirate

ADRC001 injection

Drug

Allocated patients will receive injection of 5 ml suspension including 30 million allogenic adipose-derived regenerative cells ADRC001 and injected at the same site of the lipoaspirate injection.

Other names: Liposuction, Surgical debridement of fistula tract and closure of internal orifice, Injection of lipoaspirate

Primary outcomes

  1. Healing rate (percentage)

    Time frame: at 6 and 12 months follow-up

    Clinical healing is defined as closure of the external opening(s), absence/cessation of discharge and swelling by palpation.

Secondary outcomes

  1. QoL

    Time frame: at12 months follow-up.

    functional outcome regarding quality of life, measured by Short Form SF-36 Rand questionnaire.

  2. Fecal Incontinence

    Time frame: at12 months follow-up.

    functional outcome regarding fecal incontinence, measured by Wexner Fecal Incontinence score.

  3. Risk factors for recurrence of fistula.

    Time frame: at12 months follow-up.

    Risk factors for recurrence of fistula including demography, prevoius surgery for fistula, disease duration and treatment arm.

  4. Radiological healing.

    Time frame: at12 months follow-up.

    Radiological healing, defined as no visible fistula or fluid collection more than 5 mm at MR imaging.

  5. Treatment efficacy.

    Time frame: at12 months follow-up.

    comparison of the healing rate of the fistula between patients receiving ADRC and patients receiving ADRC001 (autologous vs. allogenic cells)

  6. Cellular composition

    Time frame: at 3 months follow-up.

    Definition of the cellular compisition of the ADRC and ADRC001 regarding cellular surface markers (CD14, CD31, CD34, CD45, CD73, CD90, CD105, CD235a, HLA-ABC og HLA-DR) using flowcytometry.

  7. Transplantation-related alloantibodies

    Time frame: at12 months follow-up.

    Registration of the number of patients developing serum alloantibodies specific to donor genotypes, by assessment of anti-HLA (class I and II).

Study contacts

Contact information is provided by the study sponsor or research team.

Karam M Sørensen, Ph.D

CONTACT

[email protected]

+4565415190

Tina D Hansen

CONTACT

[email protected]

+4565415190

Sponsors and collaborators

Lead sponsor

University of Southern Denmark

Other

Registry information

Official study title

Repairing Peri-Anal Fistulas With Regenerative Cell Therapeutics

Acronym: REP-PAF

Important dates

Study start
2024
Primary completion
2027
Study completion
2028
First posted
Mar 12, 2024
Registry last updated
Nov 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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