The Effect of the Multispecies Probiotic Ecologic 825 Versus Placebo in Ulcerative Colitis Patients

NCT02361957 | Suspended

• 1 other identifier: NL46674.081.13
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

RATIONALE: The underlying etiology in inflammatory bowel diseases such as Ulcerative Colitis is not yet fully understood. Studies suggest a relation between higher intestinal permeability and aberrant changes of the epithelium. Dysbiosis of the intestinal microbiota might be the cause. Probiotics may restore the balance of the intestinal microbiota. In theory this could improve intestinal permeability and therefore reduce disease activity and maintain remission in patients with Ulcerative Colitis. OBJECTIVE: To investigate whether a specifically designed multispecies probiotic mixture (ecologic 825®), as adjuvant therapy, can contribute to an improvement of intestinal permeability, microbiota composition, disease activity and inflammatory markers in ulcerative colitis. STUDY DESIGN: 12-wk placebo-controlled randomized double-blind intervention with 2 parallel arms. STUDY POPULATION: Adults diagnosed with left sided Ulcerative Colitis or Pancolitis in remission or mild stage of the disease. For inclusion of the patients the Patient Simple Clinical Colitis Activity Index (P-SCCAI) will be used. INTERVENTION: Patients will receive either two daily dosages of 3 g of Ecologic® 825 or two daily doses of 3 g of the placebo, containing only the carrier material (both produced by Winclove Probiotics). MAIN STUDY PARAMETERS/ENDPOINTS: Main study parameter is intestinal permeability measured by several techniques: the lactulose/mannitol absorption test (L/M test), LPS levels in blood serum and faecal zonulin. Secondary, inflammation will be measured from faecal calprotectin and blood c-reactive protein (CRP) levels. Furthermore samples will be stored to measure cytokine concentrations in serum and to analyse the microbial composition of the faecal samples using the HITchip. For the disease related quality of life the irritable bowel disease questionnaire (IBD-Q) and SF-36 will be used. All parameters will be measured at three time points; t=0, t=6 and t=12 weeks.

Conditions

Ulcerative Colitis

Outcome Measures

Primary Outcomes (1)

• Intestinal permeability measured by the Lactulose Mannitol test (L/M test)

  Measured by the Lactulose Mannitol ratio in urine (L/M test)

  12 weeks

Secondary Outcomes (8)

• blood CRP levels

  6 and 12 weeks

• fecal calprotectin levels

  6 and 12 weeks

• Quality of life (measured by IBD-Q and SF36)

  6 and 12 weeks

• Intestinal permeability measured by the Lactulose Mannitol test (L/M test)

  6 weeks

• Lipopolysaccharides levels in blood

  6 and 12 weeks

Study Arms (2)

Probiotics

ACTIVE COMPARATOR

Multispecies probiotic product Ecologic 825, 2x10-9 colony forming units per gram, 6 grams per day.

Dietary Supplement: Ecologic 825

Placebo

PLACEBO COMPARATOR

Similar in appearance as the probiotics, but not containing any bacteria.

Dietary Supplement: Placebo

Interventions

Ecologic 825 DIETARY_SUPPLEMENT

Multispecies probiotic product, 2.5 x10E9 colony forming units per gram, 6 grams a day

Also known as: PRO.IB

Probiotics

Placebo DIETARY_SUPPLEMENT

Placebo

Placebo

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Diagnosed Ulcerative Colitis (left sided UC or pancolitis)
• Age 18-65 (because microbiota change at older age)
• Stable disease activity (clinical remission with CRP levels \<10mg/L and calprotectin \<100 ug/g) as measured at baseline
• Mild disease activity (P-SCCAI \<5)
• Mesalazine medication as only medication for UC with a maximum intake of 2.4 g/day

You may not qualify if:

• History of intestinal surgery that might interfere with the outcome of the study
• Diabetes Mellitus (medication dependent)
• Current use of antibiotics
• Current use of corticosteroids (30 days prior to the first baseline measurement).
• Treatment with other medication besides mesalazine (NSAIDs, topical or systemic steroids, immunosuppressive drugs or aspirin) one week prior the first baseline measurement.
• Use of other pre- and probiotics and not willing to stop these 2 weeks before the intervention period
• Hypersensitivity or allergy to milk protein, soy protein and gluten
• Alcohol abuse (male more than 14 servings a week, female more than 7 servings a week)
• Female patients: currently pregnant or breast-feeding or intending to become pregnant during the study
• Patients foreseen to need GI surgery during the study period
• Patients with a history of cancer

Sponsors & Collaborators

• Wageningen University: lead

Study Sites (1)

Gelderse Vallei Hospital

Ede, Netherlands

Location

MeSH Terms

Conditions

Colitis, Ulcerative

Condition Hierarchy (Ancestors)

Colitis; Gastroenteritis; Gastrointestinal Diseases; Digestive System Diseases; Inflammatory Bowel Diseases; Colonic Diseases; Intestinal Diseases

Study Officials

• Nicole De Roos, PhD

  Wageningen UR

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 15, 2015
• First Posted: February 12, 2015
• Study Start: November 1, 2014
• Primary Completion: December 1, 2015
• Study Completion: December 1, 2015
• Last Updated: August 28, 2015

Record last verified: 2015-08

Locations

NL (1)