Viewing Study NCT04348760



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Last Modification Date: 2024-10-26 @ 1:32 PM
Study NCT ID: NCT04348760
Status: COMPLETED
Last Update Posted: 2020-04-17
First Post: 2020-04-14

Brief Title: Study of Inflammatory Markers and Symptom Severity in Personalized Nutritional Intervention in IBS
Sponsor: GEK Srl
Organization: GEK Srl

Study Overview

Official Title: Study of Two Inflammatory Cytokines BAFF and PAF and Their Clinical Relevance Before and After a Personalized Nutritional Intervention in IBS Subjects
Status: COMPLETED
Status Verified Date: 2020-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Irritable Bowel Syndrome IBS is a widespread disease with variable symptoms that have an important impact on the quality of life Despite the prevalence of IBS its etiology and pathophysiology are still to be fully understood but immune response is known to be involved In this study the investigators researched the variation of two specific cytokines B-cell activating factor BAFF and platelet-activating factor PAF the levels of food-specific IgG and the symptom severity using Irritable Bowel Syndrome - Symptom Severity Score IBS-SSS following a personalized an unrestricted-calorie diet
Detailed Description: The investigators enrolled 30 subjects with diagnosis of IBS according to Rome-IV criteria whose inflammatory markers were measured at baseline and after 6 weeks of dietary intervention The subjects were monitored in a general practice outpatient setting GP and nutritional advice was offered remotely via two telephone sessions with a nutritionist The researchers investigated the variation of two specific cytokines B-cell activating factor BAFF and platelet-activating factor PAF the levels of food-specific IgG and the symptom severity using Irritable Bowel Syndrome - Symptom Severity Score IBS-SSS

Data monitoring was ensured by an external monitor Hippocrates Research Genova Italy

All data entry was in accordance with GCP protocol and AE were classified using CTCAE 40

Study Oversight

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