Irritable Bowel Syndrome Archives - Healthentia https://healthentia.com/tag/irritable-bowel-syndrome/ Thu, 21 Dec 2023 11:40:15 +0000 en-US hourly 1 https://healthentia.com/wp-content/uploads/2020/04/cropped-favicon_512-32x32.png Irritable Bowel Syndrome Archives - Healthentia https://healthentia.com/tag/irritable-bowel-syndrome/ 32 32 193384636 IBS study https://healthentia.com/ibs-study/ Tue, 14 Nov 2023 12:33:40 +0000 https://healthentia.com/?p=20155 Study Description The IBS study is a prospective, randomised, double-blind, placebo controlled, multicentre, parallel group, phase II study. The study will recruit 130 patients across 13 centres in Belgium and they will undergo 5 study visits, plus a follow-up phone call (if they agree to free-access to the product for 4 additional weeks) with a...

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Study Description

The IBS study is a prospective, randomised, double-blind, placebo controlled, multicentre, parallel group, phase II study. The study will recruit 130 patients across 13 centres in Belgium and they will undergo 5 study visits, plus a follow-up phone call (if they agree to free-access to the product for 4 additional weeks) with a total duration of 14 weeks.

Study Details

  • Type:  Prospective, randomized, double blind, placebo, controlled
  • Disease:  Irritable Bowel Syndrome
  • Sites: 13 Sites across Belgium
  • Start:  Phase 2: 30 Nov 2023
  • Population: 130 patients
  • Duration: 14 weeks

Study Design & Method

IBS is a common chronic gastrointestinal condition that affects approximately 10-20% of adults in Western countries for more than 10 years. Patients with IBS experience chronic, episodic abdominal pain/discomfort, bloating and constipation and/or diarrhoea. Over 80% of individuals with IBS report food-related symptoms leading in the 70% of these patients to self-imposed food restrictions and/or modifications of their diet.The study consists of a 2-week run-in period (between V0 and V1) followed by an 8-week treatment period with daily DDI-IBS-001 (between V1 and V3). At the V3, patients will be divided into responders and non-responders based on their global symptoms’ relief score, completion of electronic patient-reported outcomes (ePRO) and study product compliance.

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