Viewing Study NCT03200093



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Last Modification Date: 2024-10-26 @ 12:26 PM
Study NCT ID: NCT03200093
Status: TERMINATED
Last Update Posted: 2021-04-26
First Post: 2017-06-23

Brief Title: Oral Vancomycin for Preventing Clostridium Difficile Recurrence
Sponsor: Rochester General Hospital
Organization: Rochester General Hospital

Study Overview

Official Title: Secondary Prophylaxis With Oral Vancomycin for Clostridium Difficile Recurrence A Randomized Control Study
Status: TERMINATED
Status Verified Date: 2021-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Low recruitment due to few eligible participants
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study evaluates the role of oral vancomycin in the prevention of recurrent Clostridium difficile for hospitalized patients receiving systemic antibiotic therapy Half of participants will receive oral vancomycin daily while the other half will receive a placebo
Detailed Description: Clostridium difficile colitis is a significant cause of morbidity and mortality among hospitalized patients Following the first episode up to 15 of people experience recurrent disease A major risk factor for recurrent disease is exposure to systemic antibiotics

Oral vancomycin given four times daily is one of the treatments for Clostridium difficile infection it is not known if giving oral vancomycin at a lower dose such as once daily may help prevent recurrences Oral vancomycin may be most helpful in preventing recurrences when given to patients at greatest risk of recurrent disease such as when they are receiving systemic antibiotics

To evaluate this the investigators propose comparing the rates of recurrent Clostridium difficile infection in patients who receive oral vancomycin with systemic antibiotics to when patients take systemic antibiotics alone

Study Oversight

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