Safety and Efficacy of Injection of Human Placenta Mesenchymal Stem Cells Derived Exosomes for Treatment of Complex Anal Fistula

Last updated: November 1, 2022
Sponsor: Tehran University of Medical Sciences
Overall Status: Active - Recruiting

Phase

1/2

Condition

Rectal Disorders

Treatment

N/A

Clinical Study ID

NCT05402748
IRCT20211212053361N1
  • Ages 18-70
  • All Genders

Study Summary

Study aim:

Safety of Human Placenta Mesenchymal Stem Cells Derived Exosomes for treatment of complex Anal Fistula 2.Efficacy of Human Placenta Mesenchymal Stem Cells Derived Exosomes for treatment of refractory Anal Fistula 3.Fistula changes in MRI studies, 12 weeks after treatment 4.Evaluation of quality of life in perianal fistula patient's questionnaire score before and 12 weeks after treatment

Participants/Inclusion and exclusion criteria:

inclusion Criteria : 1.Age between 18-70 years old 2.Occurrence of complex perianal fistula 3.Informed consent Exclusion Criteria: 1.Active inflammatory bowel disease 2.Synchronous perianal abscess 3.Alcohol,narcotic and stimulant consumption 4.Having active Hepatitis B,C,HIV or TB 5.Peregnancy and lactation 6.Uncontrolled diabetes mellitus 7.Evidence of surgical contraindication 8.Psychological disorders and noncooperative patient

Intervention groups:

Human Placenta Mesenchymal Stem Cells Derived Exosomes injected in fistula tract of patients with complex perianal Fistula in 3 weekly episodes and it's safety and efficacy was evaluated.

Design:

this study includes two separate groups of cases and controls each consisting of 40 participants randomly allocated for the phase 2 of clinical trial.

Settings and conduct:

Patients with complex perianal fistula referred to Imam Khomeini hospital, will be included in the study if they contain inclusion criteria. The fistula was evaluated by clinical examination and MRI and patients fill the quality of life questionnaire. Exosome injections are performed weekly for consecutive three weeks. Patients will reexamined and fill the questionnaire and MRI will done 12 weeks later. Recent findings will compare with the initial data. During this period, patients are examine for complications.

Main outcome variables:

Discharge amount; External orifice re-epithelialization ; Inflammation, discharge and abscess larger than 2 cm in MR imaging; Quality of life questionnaire score, Inflammatory markers such as CRP, IL-6, TNF-a, calprotectin

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age between 18-70 years old
  2. Occurrence of complex perianal fistula
  3. Informed consent

Exclusion

Exclusion Criteria:

  1. Active inflammatory bowel disease
  2. Synchronous perianal abscess
  3. Alcohol,narcotic and stimulant consumption
  4. Having active Hepatitis B,C,HIV or TB
  5. Peregnancy and lactation
  6. Uncontrolled diabetes mellitus
  7. Evidence of surgical contraindication
  8. Psychological disorders and noncooperative patient

Study Design

Total Participants: 80
Study Start date:
December 22, 2021
Estimated Completion Date:
March 22, 2023

Connect with a study center

  • Division of Colorectal Surgery, Department of Surgery, Tehran University of Medical Sciences, Tehran, Iran

    Tehran, 1419733141
    Iran, Islamic Republic of

    Active - Recruiting

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