Autologous Muscle Fiber Fragment Injections

This is an interventional treatment trial for Fecal Incontinence focused on measuring low anal pressures, passive incontinence, bowel movements, sphincter muscle Read More

Inclusion Criteria:

• 18 years of age
• participants must experience 4 or more Fecal Incontinence (FI) episodes per 2 week period
• participants must score >10 on Cleveland Clinic Fecal Incontinence Severity Scoring System (CCIS)
• participants must have had symptoms for at least 12 months
• participants who have failed standard medical and surgical treatments for FI
• participant will undergo anorectal manometry (ARM) testing
• participants will undergo endoscopic anal ultrasound and demonstrate an anatomic defect of the anal sphincter complex of at least 30 degrees
• women of childbearing potential must use acceptable contraceptives during this study

Exclusion Criteria:

• participants with symptomatic anorectal disease including symptomatic hemorrhoid disease, anal fissure or fistula causing symptoms such as bleeding, swelling, pain, or drainage
• participants with pre-existing ano-rectal pain of any cause
• participants with incontinence of flatus only
• chronic watery diarrhea which is the primary cause for fecal incontinence
• acute or chronic anorectal infections (including proctitis, recurrent abscesses, fistulae)
• presence of anorectal tumors
• active proctitis or inflammatory bowel disease
• previous injection of internal anal sphincter (IAS) with bulking agents
• participants requiring immunosuppression or who have any malignant disease within 3 years of enrollment
• participants with a defined bleeding disorder diagnosed and treated by a hematologist
• other exclusions include history of pelvic radiation, rectal prolapse, anorectal malformations, anorectal surgery within the previous 12 months, or treatments using injection or infrared coagulation for treatment of hemorrhoids
• participants with neurologic disease characterized by significant peripheral neuropathy or spinal cord dysfunction
• women who are pregnant, breastfeeding, or have had a child within the last year
• participants with a history of unstable cardiac function (New York Heart Association Functional Classification III or IV) or unstable pulmonary function requiring home oxygen, or abnormal kidney function (Cr >1.5 mg/dl or on dialysis) or uncontrolled diabetes (Hemoglobin A1C > 8 mg/dl)
• participants with anemia (hemoglobin <10g, increased alanine aminotransferase (ALT) and aspartate aminotransferase (AST) >2 times normal) or increased bilirubin >1.5mg/dl
• participants with Hepatitis B or C, or human immunodeficiency virus (HIV)-1 or 2
• rectal prolapse
• vaginal prolapse beyond the hymen
• unable to understand informed consent information even with provision of a medical translator