The effect of oral administration of a multispecies probiotic product in healthy volunteers and ileostomy patients; double-blind, placebo-controlled, cross-over trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN45167712

Enrollment

Registered

2005-09-12

Start date

2004-08-01

Completion date

Unknown

Last updated

2015-01-13

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

Conditions

Healthy volunteers and ileostomy patients after ulcerative colitis Digestive System Ulcerative colitis

Interventions

Administration of probiotics or placebo

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 10 healthy volunteers and 10 ileostomy patients after ulcerative colitis

Exclusion criteria

Exclusion criteria: Use of antibiotics and/or probiotics within 2 weeks prior to randomisation

Design outcomes

Primary

Measure	Time frame
Tolerance of study product and gut flora modification	—

Secondary

Measure	Time frame
Side effects, discomfort scores (visual analogue scale [VAS] scale)	—

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026