Autologous Stem Cells Derived From Lipoaspirates for the Non-Surgical Treatment of Complex Perianal Fistula

Cellerix

Status and phase

Unknown

Phase 2

Conditions

Anal Fistula

Treatments

Procedure: Non-surgical autologous implant of ASCs

Study type

Interventional

Funder types

Industry

Identifiers

NCT00115466

GX401/TCFIS

Nr. 04-0211

Details and patient eligibility

About

This comparative, multicentre, randomised clinical trial is designed with two parallel groups that will follow a treatment either with an autologous implant of ASCs (Adipose Derived Stem Cells) and fibrin glue (tissue adhesive material) or with fibrin glue alone for the non-surgical treatment of complex perianal fistula.

Full description

Comparative, multicentre, randomised clinical trial, designed with two parallel groups that will follow a treatment either with an autologous implant of ASCs (Adipose Derived Stem Cells) and fibrin glue (tissue adhesive material) or with fibrin glue alone for the NON-SURGICAL treatment of complex perianal fistula. The closure/healing of the fistula will be evaluated periodically, and it will be considered completely closed if there is no suppuration from the external orifice and re-epithelialisation can be observed at 8 weeks after the administration of the randomised therapy.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients of both sexes older than 18 years of age.
Patients with a complex perianal fistula pathology which we define as the subjects that fulfil some of the following conditions:
- No palpation of the fistula tract beneath the perianal skin.
- A tract that is parallel to the rectum on exploration with a stylet.
- Associated faecal incontinence.
- Risk factors of anal incontinence.
- At least one previous operation for a fistulous disorder.
- Suprasphincteric trajectories
- Rectovaginal fistula
- Prior diagnosis of Crohn's disease.
Patients from whom written informed consent has been obtained for them to participate in the study prior to performing any procedure described in the study.
Patients that have already been subjected to a colonoscopy within a period of up to 6 months prior to the study.

Exclusion criteria

Patients that are extremely thin who should not be subjected to liposuction.
Known allergy to local anaesthetics or to bovine proteins
History of neoplasia in the past 5 years.
Patients with a diagnosis of active Tuberculosis at the moment of inclusion.
Patients with prior positive markers for any of the following pathogens: Hepatitis B and C, HIV-1 or HIV-2.
Any other medical condition that in the judgement of the investigator could interfere with their optimal participation in the study or produce a significant risk to the patient.
Patients that have participated in another study in the 30 days prior to this one or that have planned to participate simultaneously in another study.
Patients that have not given their informed consent to participate in this study.
Psychiatric disorder or other factors that in the judgement of the investigator could complicate the participation of the patient in the study.
Breast feeding, gestation or intention to become pregnant up to 6 months after finalising their participation in the study, or that are not using adequate methods of contraception during the same period.