Viewing Study NCT06609746



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06609746
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-14

Brief Title: Effectiveness of Thyme in the Management of Clinical Symptoms in Patients with Irritable Bowel Syndrome
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Low FODMAP Fermentable Oligo- Di- Mono-saccharides and Polyols Diet with Thyme on Clinical Symptoms and Quality of Life in Patients with Irritable Bowel Syndrome
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to learn if thyme supplement enhances the effects of a low FODAMP diet on reducing clinical symptoms and improving the quality of life of patients with irritable bowel syndrome or not

The main questions it aims to answer are

1 Does consumption of thyme reduce the severity score of clinical symptoms in patients with irritable bowel syndrome
2 Does consumption of thyme increase the quality of life score in patients with irritable bowel syndrome Researchers will compare thyme supplementation with placebo to see if thyme supplement enhances the effects of a low FODAMP diet on clinical symptoms and quality of life in patients with irritable bowel syndrome

Participants will

1 Receive thyme supplement plus a low FODMAP diet or placebo with low FODMAP diet for 8 weeks
2 Recorde 3 days 1weekend and 2 workday dietary recalls at week 4 and week 8 to assess adherence to the low FODMP diet
3 Visit the clinic at the beginning of the study and the end of the study for a check-up and score record
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None