Digestive Enzyme Formulation Intervention in Irritable Bowel Syndrome Patients Who Previously Clinically Responded to Mediterranean Low FODMAP Diet: A Single-Arm Clinical Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Irritable bowel syndrome (IBS) is a highly prevalent chronic functional gastrointestinal disorder. The cardinal symptoms include abdominal pain, flatulence, bloating, and changes in bowel habits related to stool frequency and consistency, in the absence of detectable structural and biochemical abnormalities1,2. The prevalence is estimated at 5-10% among different ethnicities3. A low FODMAP diet is the most common dietary intervention with clinically proven benefits in symptom management and quality of life improvement of patients with Irritable Bowel Syndrome (IBS)4. Recently, a dietary digestive enzyme formulation (FODZYME©) claims similar efficacy in symptom management based on an ex-vivo study5. The study aims to examine the clinical efficacy of this formulation in managing IBS symptoms in patients who have previously clinically responded to a low FODMAP diet.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Provision of written informed consent.

• Commitment to availability throughout the study period.

• Patients who fulfilled the Rome IV criteria for IBS (IBS-D, IBS-M, IBS-U) participated in the two-arm clinical trial (ClinicalTrials.gov ID: NCT03997708) as responders to the Mediterranean Diet Adjusted to Low FODMAP (MED-LFD) (if their symptoms recurred -with IBS-SSS \> 175- one year after their initial response to the dietary intervention).

• Subjects randomized to the MED-LFD arm of the previous study who could not adhere to the dietary intervention.

Locations
Other Locations
Greece
Attikon University General Hospital
RECRUITING
Athens
Attikon University General Hospital
RECRUITING
Chaïdári
Contact Information
Primary
AREZINA KASTI, PhDc
kastiare@yahoo.gr
6942917860
Backup
Konstantinos Triantafyllou, Professor
ktriant@med.uoa.gr
6977402690
Time Frame
Start Date: 2024-12-10
Estimated Completion Date: 2026-03-30
Participants
Target number of participants: 40
Treatments
Experimental: digestive enzymes group
Patients will be instructed to use a powder formulation according to manufacturer instructions and according to the meals that they consume per day, for 1 month. To reduce the placebo effect, patients will be misinformed that half will take a placebo formulation, randomly.
Related Therapeutic Areas
Sponsors
Leads: Attikon Hospital

This content was sourced from clinicaltrials.gov