Odense University Hospital
Odense, 5000, Denmark
Location status: Recruiting
Location contact
Karam M Sørensen, Ph.D
CONTACT
Karam M Sørensen, Phd
PRINCIPAL_INVESTIGATOR
Tina D Hansen
CONTACT
NCT Number: NCT06303752
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Odense, 5000, Denmark
Location status: Recruiting
Karam M Sørensen, Ph.D
CONTACT
Karam M Sørensen, Phd
PRINCIPAL_INVESTIGATOR
Tina D Hansen
CONTACT
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.
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:
Exclusion criteria
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
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
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.
Time frame: at12 months follow-up.
functional outcome regarding quality of life, measured by Short Form SF-36 Rand questionnaire.
Time frame: at12 months follow-up.
functional outcome regarding fecal incontinence, measured by Wexner Fecal Incontinence score.
Time frame: at12 months follow-up.
Risk factors for recurrence of fistula including demography, prevoius surgery for fistula, disease duration and treatment arm.
Time frame: at12 months follow-up.
Radiological healing, defined as no visible fistula or fluid collection more than 5 mm at MR imaging.
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)
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.
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).
Contact information is provided by the study sponsor or research team.
Karam M Sørensen, Ph.D
CONTACT
Tina D Hansen
CONTACT
University of Southern Denmark
Other
Repairing Peri-Anal Fistulas With Regenerative Cell Therapeutics
Acronym: REP-PAF
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.
Published trials that share one or more normalized conditions with this study.
NCT05243966
Abdominal Wound Dehiscence, Anal Fistula
Phoenix, Arizona, United States
View Trial DetailsNCT05974280
Anal Fistula, Crohn Disease
Nantes, France
View Trial DetailsNCT07477496
Anal Fistula, Anal Fistula Surgery
Athens, Greece
View Trial DetailsNCT04190862
Anal Fistula, Digestive System Diseases
New York, United States
View Trial Details