Viewing Study NCT00179582



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00179582
Status: TERMINATED
Last Update Posted: 2019-02-27
First Post: 2005-09-13

Brief Title: Dose Ranging Study With the Probiotic Combination VSL3 in Diarrhea IBS
Sponsor: Beth Israel Deaconess Medical Center
Organization: Beth Israel Deaconess Medical Center

Study Overview

Official Title: A Randomized Multi-center Double-blind Placebo Controlled Dose Ranging Study With VSL3 in Diarrhea Predominant IBS Patients
Status: TERMINATED
Status Verified Date: 2019-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Lack of enrollment
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To evaluate the effects of VSL3 on symptoms associated with diarrhea predominant IBS
Detailed Description: The study will evaluate 2 doses of VSL3 and placebo over a 4 week period in patients presenting with diarrhea predominant IBS symptoms

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
Secondary IDs
Secondary ID Type Domain Link
VSL1 None None None