Efficacy of Loperamide for C. Difficile Colitis and Other Diarrheal Diseases Associated With Antibiotic Therapy

Clostridium Difficile Clinical Trial

— loperamide  

Official title:

Study of the Efficacy of Loperamide in Treating Patients for Clostridium Difficile Colitis and Diarrheal Disease of Unknown Cause Associated With Prior Antibiotic Therapy.

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT00591357
• Other study ID #: H-21387
• Secondary ID: Clostridium diff
• Status: Suspended
• Phase: Phase 4
• First received: December 31, 2007
• Last updated: May 2, 2016
• Start date: October 2007

Study information

• Verified date: May 2016
• Source: VA Medical Center, Houston
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

To determine whether symptomatic treatment of the diarrhea in CDAD reduces morbidity and mortality of this serious nosocomial infection in patients who have antibiotic-associated diarrhea. Both C. diff positive and negative patients will be included.

Description:

Colitis due to Clostridium difficile has been increasingly recognized as a serious nosocomial problem. Recommended therapy is with metronidazole, 500 mg four times daily for 10 days. About 80% of patients respond to this therapy. However, the response may be be delayed, in which case debilitation due to diarrhea progresses. The 20% who do not respond tend to be sicker to start, and debilitation due to diarrhea is a severe problem. In reviewing the medical literature, we discovered that the earliest papers on C. difficile colitis emphasized symptomatic therapy with 'lomotil' (diphenoxylate with atropine).

Treatment to suppress the diarrhea fell out of favor in the late 1970's because of the theoretical consideration that it was better to expel than to retain the bacterial toxins. However, the patients who are affected by C. difficile colitis are increasingly elderly and debilitated, and suffer substantial morbidity from the diarrhea. We have shown that the 90-day associated mortality is >20%.

Loperamide is a standard treatment for diarrhea, and is available over the counter under the name, Imodium. Based on a few anecdotal reports, this drug is regarded as contraindicated in patients whose diarrheal disease is bacterial. But it is used widely, and generally without any diagnosis being established. We now propose to administer loperamide or placebo to patients with CDAD in order to determine whether the antidiarrheal drug reduces morbidity associated with the infection. We will monitor our patients closely both to observe potential benefits and/or adverse events.

In the addendum, we propose to include patients who have antibiotic-associated diarrheal disease that is not due to C. difficile. There are many patients who have antibiotic-associated diarrheal disease who test negative for C. difficile. We believe that these patient may benefit from loperamide treatment as well.

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 120
• Est. primary completion date: December 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with diarrheal stools considered to be antibiotic associated

Exclusion Criteria:

• Inability of sign consent

• Patient with other known gastrointestinal disease

• Patients receiving tube feeding or fecal incontinence prior to receiving antibiotics

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Antibiotic-Associated Diarrhea
• Clostridium Difficile
• Diarrhea

Intervention

Drug:
• loperamide
4 mg PO initially and 2 mg after each water stoll not to exceed 10 mg qd
• placebo
4 mg PO initially and 2 mg after each water stoll not to exceed 10 mg qd

Locations

Country	Name	City	State
United States	VAMC	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
VA Medical Center, Houston

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determin symptomatic treatment of diarrhea with loperamide in antibiotic associated diarrhea		2 years	Yes
Secondary	To measure the safety and efficacy of loperamide in the control of antibiotic associated diarrhea in hospitalized patients		2 years	Yes