A Study of Efficacy, Safety and Durability of Fecal Microbiota Transplantation in Adult Patients With Slow Transit Constipation
Overview
- Phase
- Phase 2
- Intervention
- Fecal microbiota transplantation (FMT)
- Conditions
- Slow Transit Constipation
- Sponsor
- Jinling Hospital, China
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Proportion of patients having on average three or more SCBMs/week
- Last Updated
- 9 years ago
Overview
Brief Summary
The purpose of this study is to evaluate the effect of fecal microbiota transplantation in adults with slow transit constipation.
Detailed Description
Constipation is a chronic disease estimated to affect about 10% - 15% of the worldwide general population. Constipation frequency appears to augment with increasing age, particularly after 65 years old. Recent evidence in the literature and collected in our laboratory confirm that constipation can be a consequence of intestinal dysbiosis, with an increase of potentially pathogenic microorganisms and a decrease of potentially beneficial microorganisms. These alterations may affect the motility and metabolic environment of colon, especially the production of short chain fatty acids (SCFAs). A new and under-explored method to manipulate the gastrointestinal microbiota involves fecal microbiota transplantation (FMT). There has been growing interest in the use of fecal microbiota for the treatment of patients with chronic gastrointestinal infections (e.g. CDI) and other extraintestinal conditions (e.g. IBD). Similarly, we suppose that reshaping the gut microbiome with FMT would be effective for patients with slow transit constipation.
Investigators
Jianfeng Gong
Associate professor
Jinling Hospital, China
Eligibility Criteria
Inclusion Criteria
- •Chronic constipation according to Rome III criteria, defined as two or fewer spontaneous, complete bowel movements (SCBMs) per week for a minimum of 6 months;
- •Age ≥ 18 years;
- •BMI: 18.5-25 kg/m2;
- •Slow colonic transit confirmed by colonic transit test (colonic transit time (CTT) \> 48 hours);
- •Normal anorectal manometry with no evidence of dyssynergia and confirmed ability to expel rectal balloon;
- •No radiographic evidence of functional (i.e. pelvic floor dyssynergia) or anatomical (i.e. significant rectocele and intussusception) impediment to the expulsion of the radio-opaque contrast;
- •Disease duration \> 1 year;
- •Traditional treatment with dietary modification, laxatives (including osmotic and stimulant laxatives), and biofeedback tried over the past 6 months without success;
Exclusion Criteria
- •Bowel constipation due to innate factor (i.e. megacolon) or secondary interventions (i.e. drugs, endocrine, metabolic, neurologic or psychologic disorders);
- •History or evidence of gastrointestinal diseases (i.e. obstruction, cancer, inflammatory bowel diseases) ;
- •Previous abdominal surgery, except cholecystectomy, appendicectomy, tubal ligation and cesarean section;
- •Previous proctological or perianal surgery;
- •A constipation condition meeting the Rome III criteria for IBS or functional abdominal pain syndrome;
- •Pregnant or breast-feeding women;
- •Infection with enteric pathogen;
- •Usage of probiotics, prebiotics and/or synbiotics within the last month;
- •Usage of antibiotics and/or PPIs within the last 3 months;
- •Smoking or alcohol addiction within the last 3 months;
Arms & Interventions
Fecal microbiota transplantation (FMT)
Patients included will receive standard FMT, and then will be followed up for 24 weeks.
Intervention: Fecal microbiota transplantation (FMT)
Fecal microbiota transplantation (FMT)
Patients included will receive standard FMT, and then will be followed up for 24 weeks.
Intervention: Vancomycin and bowel lavage
Outcomes
Primary Outcomes
Proportion of patients having on average three or more SCBMs/week
Time Frame: 24 weeks
Proportion of patients having on average three or more spontaneous, complete bowel movements (SCBMs) per week was evaluated at baseline and over the week interval 3-4, 9-12 and 21-24.
Secondary Outcomes
- Constipation-related symptoms assessments(24 weeks)
- Bowel habit assessments(24 weeks)
- Quality-of-Life assessments(24 weeks)
- Colonic transit time measurements(24 weeks)
- Usage of laxatives or enemas as rescue medication(24 weeks)
- Adverse events(24 weeks)