Skip to content

Proof of concept clinical trial of safety and biological activity of Bifidobacterium Longum NCC 2705 in gluten sensitivity

Proof of concept clinical trial of safety and biological activity of Bifidobacterium Longum NCC 2705 in gluten sensitivity - Probiotic BL NCC 2705 and gluten sensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46135
Enrollment
32
Registered
2018-10-26
Start date
2018-11-09
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

celiac disease gluten sensitivity

Interventions

The active product is a food supplement for human consumption. It contains 1.0x10^10 cfu of the probiotic strain Bifidobacterium longum NCC 2705 (BL NCC2705) premixed with a carrier which is maltode

Sponsors

Nestec
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Willing and able to sign written informed consent prior to trial entry 2. Male or female adults at a minimum age of 18 3. For NCGS: self-reported gluten sensitivity on gluten free diet for at least 6 weeks with self-reported significant symptomatic improvement 4. For CD: confirmed serologic and histologic diagnosis of CD and on GFD for at least 12 months with self-reported significant symptomatic improvement 5. Body Mass Index (BMI) within the range 18 * 30 kg/m2 6. Willing and able to comply with study procedures and restrictions 7. In good health as determined by a medical history and medical examination

Exclusion criteria

Exclusion criteria: 1) Documented IgE-mediated food allergy 2) Subjects following an overly imbalanced or restrictive diet as per nutritional advice 3) Concurrent systemic disease and/or laboratory abnormalities considered by investigators to be detrimental for the participants safety or potentially interfering with the study procedures and/or study outcomes 4) Concurrent organic GI pathology other than benign polyps, diverticulosis, hemorrhoids, lipomas and melanosis coli 5) Previous abdominal surgery with the exception of hernia repair, appendectomy, caesarian section, tubal ligation, hysterectomy, hemorrhoidectomy 6) Patients who received antibiotics in the previous 2 weeks 7) women of childbearing potential not willing to use an effective contraception method

Design outcomes

Primary

MeasureTime frame
1) Adverse Events (AE) incidence, type, severity and causal relationship to the investigational product 2) GI scores from a Visual Analogue Scale (VAS) over both treatment periods at home (i.e. from day 1 to day 3) for each symptom of interest (i.e. 1) nausea, 2) vomiting, 3) diarrhea, 4) audible bowel sounds, 5) flatulence, 6) abdominal cramping)

Secondary

MeasureTime frame
1) Concentration of serpin in duodenal aspirates 2) Concentration of BL NCC 2705 in duodenal aspirates 3) Inhibition of the elastase activity in duodenal aspirates 4) Concentration immunogenic (33-mer) gluten-derived peptides in duodenal aspirates following a 3g gluten containing meal 5) Inhibition of glutenasic activity in duodenal aspirates 6) Urinary excretion of immunogenic (33-mer) gluten-peptides following the gluten-containing meal

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)