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Impact of Symprove in irritable bowel syndrome

A prospective, single-arm, decentralised, real-world evidence pilot study to assess the impact of Symprove in irritable bowel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10344823
Enrollment
150
Registered
2026-05-20
Start date
2026-04-29
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Irritable bowel syndrome (IBS) Digestive System

Interventions

All participants will receive a 12-week course of Symprove (70 ml per day), a water-based solution that contains billions of live and active bacteria. Participants will also complete study surveys at

Sponsors

Symprove Ltd
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Adults (18-75 years) in the UK who have IBS, either self-diagnosed or medically diagnosed 2. Experiencing regular symptoms related to IBS (e.g., tummy pain, constipation, diarrhoea, bloating)

Exclusion criteria

Exclusion criteria: 1. Currently taking probiotics or prebiotics supplements (e.g. Bimuno) or yogurts containing probiotics (e.g., Yakult, Actimel) 3. Taken Symprove in the last 3 months 4. Taken antibiotics in the last 4 weeks 5. Diagnosed with gut conditions other than Irritable Bowel Syndrome, such as inflammatory bowel disease (e.g., Crohn’s disease or ulcerative colitis), coeliac disease, hepatitis, gallstones, acid reflux/dyspepsia 6. Received gastrointestinal surgery, cancer treatment or been hospitalised in the last 6 months 7. Diagnosed with any significant or unstable psychological issues (such as depression, bipolar illness, psychosis) 8. Diagnosed with any significant heart, lung or kidney issues 9. Currently pregnant or breastfeeding 10. Patients taking part in other interventional research where they are receiving treatment

Countries

England, United Kingdom

Contacts

Public ContactLauren Hayman
support@peopleforresearch.co.uk+44 (0)117 9210008

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 11, 2026