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Adipose Tissue Injection for the Treatment of Complex Cryptoglandular Perianal Fistula (AdiTiF)

Primary Purpose

Anal Fistula

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Injection of autologous freshly collected adipose tissue
sham
Sponsored by
Hospital Mutua de Terrassa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anal Fistula

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients over 18 years
  • Anal fistula with suppuration for more than 6 weeks and less than 1 year, that have not received any previous treatment or at most: curettage and drainage placement
  • Complex cryptoglandular anal fistula: medium or high transsphincteric fistula, suprasphincteric fistula and extra sphincter fistula, shown by endoanal ultrasound.
  • Low transsphincteric fistulas in patients with fecal incotinence.
  • Any cryptoglandular anal fistula with risk factors for anal incontinence: anterior location fistula in women, history of pelvic surgery (hysterectomy, rectal resection), history of pelvic radiotherapy or previous anal surgery
  • Draining with Seton placed >2 weeks before surgery and present at the time of treatment
  • Disposition and ability to comply with the study protocol
  • Signed informed consent

Exclusion Criteria:

  • Patients diagnosed with inflammatory bowel disease
  • Previous history of perianal fistula treated with any surgery different than curettage and seton placement (this include any type of surgery with curative intention, i.e. flap, lift technique, Radiofrequency, laser, stem cells, Filac, etc)
  • Presence of Rectovaginal fistula
  • Technical impossibility for lipoaspirate (liposuction) technique.
  • Presence of perianal collections larger than 2cm
  • Presence of several paths from 1 internal hole only
  • Presence of secondary fistula paths or tracts
  • Perianal surgery necessary at the time of planning the fistula treatment, for reasons other than fistula.
  • Major surgery needed within 28 days of recruitment
  • Immunomodulator treatment or corticotherapy in a previous period of 6 months
  • Stoma patients
  • Serious medical or psychiatric illness that requires frequent hospitalization.
  • Pregnancy, pregnancy plans or breastfeeding in the next 12 months
  • Active smokers, or ex-smokers of less than 3 months

Sites / Locations

  • Hospital Universitari Mutua TerrassaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Control group

Experimental group

Arm Description

Outcomes

Primary Outcome Measures

Complete fistula healing
Comparison of the proportion of cases with complete fistula healing within 24 weeks of the intervention, defined as the absence of drainage through the external orifice, its complete reepithelialization and the absence of collections confirmed by endoanal ultrasound.

Secondary Outcome Measures

Patient's Quality of life
Improvement in quality of life (measured with the Quality of Life in Patients with Anal Fistula Questionnaire, QoLAF). Score from 14 to 70, where 14 means "no quality of life alteration" and 70 means "severe quality of life alteration".
Patient's Subjective Perception
Improvement in patient subjective evaluation using a Visual Analogue Scale (VAS). Score from 0 to 10, where 0 means "no problem" and 10 means "severe problem and alteration of my quality of life".
Fistula severity
Improvement in fistula severity according to the Complexity Fistula score (CFS). Score from 3 to 15, where 3 means "low complexity" and 15 means "high complexity"
Adverse events
Evaluation of the safety by the incidence of adverse events and serious adverse events.

Full Information

First Posted
February 7, 2021
Last Updated
March 1, 2023
Sponsor
Hospital Mutua de Terrassa
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1. Study Identification

Unique Protocol Identification Number
NCT04790123
Brief Title
Adipose Tissue Injection for the Treatment of Complex Cryptoglandular Perianal Fistula
Acronym
AdiTiF
Official Title
Adipose Tissue Injection for the Treatment of Complex Cryptoglandular Perianal Fistula
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 14, 2020 (Actual)
Primary Completion Date
November 14, 2023 (Anticipated)
Study Completion Date
October 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Mutua de Terrassa

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The incidence of complex cryptoglandular anal fistula is high, it affects eminently young patients and implies an important alteration in their quality of life and high prevalence in sick leave. Its treatment remains a real challenge due to the limited efficacy of sphincter preservation techniques and the inevitable risk of faecal incontinence in those cases that require surgery. Goals: To evaluate the efficacy and safety of the injection of freshly collected autologous adipose tissue as a minimally invasive, highly reproducible alternative, without risk for the continence of the patient, and of very low cost, in the treatment of complex cryptoglandular anal fistula. Methodology: Prospective multicenter, randomized, double-blinded, parallel-group, placebo-controlled clinical trial. Randomization list for each center to ensure the balance of inter-center allocation. Patients older than 18 years with cryptoglandular anal fistula with suppuration for more than 6 weeks and less than 1 year, who have received at most: curettage and drainage placement will be included. Treatment group: injection of fresh autologous fat into the fistulous tract, after curettage and closure of the internal orifice, and after lipoaspirate fat in the abdomen and centrifugation thereof. Placebo group: curettage and closure of the internal orifice and simulated intervention in the abdomen. Evaluation: protocolized clinical history and fistula complexity score (CFS), subjective perception of its pathology, St.Marks continence score, Quality of life questionnaire (QoLAF), and endoanal 3D ultrasound, at baseline, at one week, and at 3, 6 and 12 months after the intervention. The patients and the evaluator will be blind to the treatment. Patients who cannot end up receiving treatment due to intraoperative incidents or medical decision will be excluded from the study (post randomization exclusion). In each center there will be a blind evaluator to perform the follow-ups and endoanal ultrasound.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anal Fistula

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Sham Comparator
Arm Title
Experimental group
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Injection of autologous freshly collected adipose tissue
Intervention Description
injection of fresh autologous fat, previously lipoaspirates from the patient's abdomen and centrifugated, into the fistulous tract, after curettage and closure of the internal opening.
Intervention Type
Procedure
Intervention Name(s)
sham
Intervention Description
curettage and closure of the internal orifice of the anal fistula and simulated intervention in the abdomen.
Primary Outcome Measure Information:
Title
Complete fistula healing
Description
Comparison of the proportion of cases with complete fistula healing within 24 weeks of the intervention, defined as the absence of drainage through the external orifice, its complete reepithelialization and the absence of collections confirmed by endoanal ultrasound.
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Patient's Quality of life
Description
Improvement in quality of life (measured with the Quality of Life in Patients with Anal Fistula Questionnaire, QoLAF). Score from 14 to 70, where 14 means "no quality of life alteration" and 70 means "severe quality of life alteration".
Time Frame
6 and 12 months after treatment.
Title
Patient's Subjective Perception
Description
Improvement in patient subjective evaluation using a Visual Analogue Scale (VAS). Score from 0 to 10, where 0 means "no problem" and 10 means "severe problem and alteration of my quality of life".
Time Frame
6 and 12 months after treatment.
Title
Fistula severity
Description
Improvement in fistula severity according to the Complexity Fistula score (CFS). Score from 3 to 15, where 3 means "low complexity" and 15 means "high complexity"
Time Frame
6 and 12 months after treatment.
Title
Adverse events
Description
Evaluation of the safety by the incidence of adverse events and serious adverse events.
Time Frame
3, 6 and 12 months after treatment.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients over 18 years Anal fistula with suppuration for more than 6 weeks and less than 1 year, that have not received any previous treatment or at most: curettage and drainage placement Complex cryptoglandular anal fistula: medium or high transsphincteric fistula, suprasphincteric fistula and extra sphincter fistula, shown by endoanal ultrasound. Low transsphincteric fistulas in patients with fecal incotinence. Any cryptoglandular anal fistula with risk factors for anal incontinence: anterior location fistula in women, history of pelvic surgery (hysterectomy, rectal resection), history of pelvic radiotherapy or previous anal surgery Draining with Seton placed >2 weeks before surgery and present at the time of treatment Disposition and ability to comply with the study protocol Signed informed consent Exclusion Criteria: Patients diagnosed with inflammatory bowel disease Previous history of perianal fistula treated with any surgery different than curettage and seton placement (this include any type of surgery with curative intention, i.e. flap, lift technique, Radiofrequency, laser, stem cells, Filac, etc) Presence of Rectovaginal fistula Technical impossibility for lipoaspirate (liposuction) technique. Presence of perianal collections larger than 2cm Presence of several paths from 1 internal hole only Presence of secondary fistula paths or tracts Perianal surgery necessary at the time of planning the fistula treatment, for reasons other than fistula. Major surgery needed within 28 days of recruitment Immunomodulator treatment or corticotherapy in a previous period of 6 months Stoma patients Serious medical or psychiatric illness that requires frequent hospitalization. Pregnancy, pregnancy plans or breastfeeding in the next 12 months Active smokers, or ex-smokers of less than 3 months
Facility Information:
Facility Name
Hospital Universitari Mutua Terrassa
City
Terrassa
State/Province
Barcelona
ZIP/Postal Code
08221
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pilar Arcusa
Phone
937365050
Email
parcusa@mutuaterrassa.es

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Adipose Tissue Injection for the Treatment of Complex Cryptoglandular Perianal Fistula

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