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Probiotics in Patients With Moderate-to-severe Distention/ Bloating From Systemic Sclerosis

Probiotics in Patients With Moderate-to-severe Distention/ Bloating From Systemic Sclerosis

Status
Withdrawn
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01497743
Acronym
PRISS
Enrollment
0
Registered
2011-12-22
Start date
2012-02-29
Completion date
Unknown
Last updated
2016-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scleroderma

Keywords

Scleroderma, gastrointestinal, bloating, reflux

Brief summary

Organs of the gastrointestinal tract include the mouth, throat, stomach, intestines, and anus. Patients with scleroderma often have GIT disorders. GIT disorders can be severely debilitating and even life-threatening. Some problems associated with GIT disorders may include heartburn, loss of voice or hoarseness, ulcers (open sores), difficulty swallowing, constipation, diarrhea, malabsorption (impaired absorption of nutrients from the GI tract), diminished peristalsis (decreased in the wavelike motion in the muscles of the intestines), and the inability to control your bowel movements. Probiotics are the good bacteria normally found in your digestive tract. Our group is looking at whether or not taking daily probiotics (lactobacillus) can help alleviate some of these symptoms in scleroderma patients that have GIT disorders.

Interventions

All randomized subjects will receive probiotic or matching placebo: 1 capsule orally twice daily, with meals) for the first 4 weeks. There will be a 6-week washout period, followed by 4 weeks of the alternate treatment. The subject will not be on study medication during this washout period.

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adult patient ≥18 years. 2. Patients with SSc with moderate-to-severe distention/bloating on GIT 2. scale (scale score \>1.00). 3. Stable immunosuppressive therapy(ies) for ≥ 1 month. 4. Stable PPI and/or other anti-reflux medications for ≥ 1 month. 5. Stable calcium channel blocker for ≥ 1 month. 6. Stable NSAID for ≥ 1 month. 7. Stable dose of pro-motility agent for ≥ 1 month.

Exclusion criteria

1. Recent diagnosis for small intestinal bacterial overgrowth (SIBO) during last 1 month. 2. Treatment with antibiotics within last 2 weeks. 3. Currently receiving chemotherapy (pulse cyclophosphamide). It is acceptable to be on methotrexate, mycophenolate mofetil, hydroxychloroquine, or azathioprine. 4. Severe diarrhea (Diarrhea scale score of ≥ 1.01; may suggest untreated SIBO). 5. History of inherited or acquired immunodeficiency \-

Design outcomes

Primary

MeasureTime frame
1. Proportion of patients with improvement in distention/bloating scale ≥ 0.14 at the end of 4 weeks. A change of 0.14 is the minimally important difference for this scale(9)12 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026