跳至主要内容
临床试验/NCT04790123
NCT04790123招募中不适用

Adipose Tissue Injection for the Treatment of Complex Cryptoglandular Perianal Fistula

Hospital Mutua de Terrassa2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年10月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
2
主要终点
Complete fistula healing

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Complete fistula healing

时间窗: 24 weeks

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.

次要结局

  • Adverse events(3, 6 and 12 months after treatment.)
  • Patient's Quality of life(6 and 12 months after treatment.)
  • Patient's Subjective Perception(6 and 12 months after treatment.)
  • Fistula severity(6 and 12 months after treatment.)

研究者

发起方
Hospital Mutua de Terrassa
申办方类型
Other
责任方
Principal Investigator
主要研究者

Arantxa Muñoz-Duyos

Clinical Head of the General Surgery Service. Coloproctology Unit.

Hospital Mutua de Terrassa

研究点 (2)

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