Aarhus University Hospital
Aarhus, Denmark
NCT Number: NCT06333795
This clinical trial aims to assess the safety and effectiveness of faecal Microbiota Transplantation (FMT) in improving chronic diarrhea symptoms among patients with systemic sclerosis.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Not applicable
Aarhus, Denmark
The present study aims to assess the feasibility, pilot efficacy, and safety of FMT for patients with Systemic Sclerosis.
Participants will undergo two interventions in this present study.
In the first intervention, participants are randomized 1:1 for either active FMT or Placebo. This first intervention consists of two doses of FMT with a 3-7 day gap.
In the second intervention, all participants receive 1 dose of active FMT treatment.
This study design allows researchers to evaluate the safety of FMT in this patient group, and compare the effects of FMT in the FMT-treated group vs the placebo group, to see if FMT promotes remission of Chronic diarrhea. Furthermore, researchers will be able to gain insights into whether 2 initial doses are superior to one.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Treatment is given as capsules.
Treatment is given as capsules.
Time frame: The first week after treatment.
Patient-reported measures from the schedule of side effects and telephone call 1 week after each intervention.
Time frame: The first week after treatment.
Based on self-reported data from the bowel habit diary.
Time frame: One week after each treatment
Mild adverse events (grade 1) following FMT or placebo assessed by (Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0) CTCAE v5.0.
The CTCAE grades adverse events (AEs) based on severity:
Grade 1: Mild, asymptomatic, or mild symptoms; no intervention needed. Grade 2: Moderate; requires minimal intervention; affects age-appropriate activities.
Grade 3: Severe or medically significant, not immediately life-threatening; may require hospitalization.
Grade 4: Life-threatening; urgent intervention needed. Grade 5: AE-related death. Note: Some AEs may not have all five grades available.
Time frame: At Baseline and 4 weeks after Intervention 1 & 2
Change in Gastrointestinal syndrome rating scale - irritable bowel version questionnaire (GSRS-IBS)
Time frame: At Baseline and 4 weeks after Intervention 1 & 2
Change in Wexner incontinence score.
Time frame: At Baseline and 4 weeks after Intervention 1 & 2
Change in UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract (UCLA SCTC GIT 2.0)
Time frame: Each week for a total of 26 weeks.
The patients self-reported the severity of symptoms and their impact on daily life each week on a scale from 1-5. 1 being little to no burden, 5 being most severe.
Time frame: At baseline
Transit time through the small intestine.
Time frame: At baseline
Colonic transit times
Time frame: At baseline
Total gastrointestinal transittimes
Time frame: At baseline
Ph drop from the small intestine to the colon
Time frame: At baseline and 4 weeks after first intervention
Volume of the a) small intestine and b) the colon. Volume of gas in a) the small intestine and b) the colon.
Changes in the gas volume in the small intestine and colon.
Time frame: At baseline and 4 weeks after first intervention
Changes in the rise of hydrogen and methane measured in breath test
Time frame: At baseline and between each treatment, up to 4 weeks after last intervention
Changes in faecal microbiome composition. Alfa and beta diversity determined by sequencing of the intestinal microbiome.
Time frame: At Baseline and 4 weeks after Intervention 1 & 2
Percentual change in faecal-calprotectin from before intervention to 4 weeks after each intervention.
Time frame: At baseline and between each treatment, up to four weeks after last intervention.
Changes in blood immunological parameters (including proteins) from baseline and between each treatment, at 4 weeks after intervention.
Time frame: At baseline and between each treatment, up to four weeks after last intervention.
Changes in blood immunological parameters (including markers of fibrosis) from baseline and between each treatment, at 4 weeks after intervention.
Time frame: At baseline and between each treatment, up to four weeks after last intervention.
Changes in blood immunological parameters (including circulating cytokines) from baseline and between each treatment, at 4 weeks after intervention.
Time frame: At baseline and 4 weeks after Intervention 1 & 2
Changes in Health-related Quality of life assessed with (EQ-5D-5L). Each of the five dimensions comprising the EQ-5D descriptive system is divided into five levels of perceived problems: LEVEL 1: indicating no problem LEVEL 2: indicating slight problems LEVEL 3: indicating moderate problems LEVEL 4: indicating severe problems LEVEL 5: indicating unable to/Extreme problems
An EQ-VAS from 0-100 is added, 100 being the best possible health.
Time frame: At 4 weeks after interventions 1 & 2
Patient perception of FMT treatment satisfaction was assessed by 7-point Likert scale for patients. 1: no benefits from treatment to 7 being very satisfied with treatment.
University of Aarhus
Other
Faecal Microbiota Transplantation Against Chronic Diarrhea in Patients With Systemic Sclerosis - a Randomized, Double-blinded, Safety and Pilot-efficacy Study
Acronym: FaeMiCue
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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