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Study was stopped for slow enrollment - only 2 patients, no evaluable results
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| Name | Class |
|---|---|
| Scott and White Hospital & Clinic | OTHER |
| Texas A&M University | OTHER |
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Clostridium difficile (C. difficile) can cause symptoms ranging from mild diarrhea to life-threatening colitis. Illness from C. difficile most commonly affects patients in hospitals and long-term care facilities and typically occurs after a patient has received antibiotics.
In vitro data indicate Calcium Aluminosilicate Anti-Diarrheal (CASAD) has the potential to bind TNFα, IL-1, IL-6, and IL-10 in the intestines and, therefore, may act to reduce severity of fever, leukocytosis, and bowel injury in patients with C. difficile infection. This would likely occur in conjunction with neutralization of C. difficile toxins A&B by CASAD. Computer modeling of CASAD performed by Phillips et al. at Texas A&M University supports this hypothesis.
The investigators hypothesize that adding CASAD 1.5 grams po tid to any standard-of-care therapy will reduce the duration and severity of diarrhea and other symptoms in patients with C. difficile infection.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Open Label CASAD | Experimental | Treatment with CASAD for 14 days |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Calcium Aluminosilicate Anti-Diarrheal (CASAD) | Drug | CASAD 3 500mg capsules po tid for 14 days with 4 weeks of follow up |
|
| Measure | Description | Time Frame |
|---|---|---|
| Resolution of Diarrhea | To evaluate the safety and efficacy of CASAD added to the standard-of-care for the therapy of Clostridium difficile infection (C. difficile). | 42 days |
| Measure | Description | Time Frame |
|---|---|---|
| Stools Per Day | Compare the number of liquid stools per day during treatment period | 14 days |
| Resolution of Abdominal Pain | Compare time to resolution of abdominal pain |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Aarthi Narasimhan, MD | Scott & White Memorial Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Scott & White Memorial Hospital | Temple | Texas | 76508 | United States |
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Recruiting was managed by Scott & White
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| ID | Title | Description |
|---|---|---|
| FG000 | Open Label CASAD | Treatment with Calcium Aluminosilicate Anti-Diarrheal (CASAD) for 14 days |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| 14 days |
| Absence of Relapse | Compare sustained clinical response | 42 days |
| Side-effects and Complications | Compare side-effects and complications | 42 days |
| COMPLETED |
|
| NOT COMPLETED |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Open Label CASAD | Treatment with CASAD for 14 days |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants | Participants |
| ||||||||||||||||||||
| Age Continuous | Mean | Standard Deviation | years |
| |||||||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||||||
| Region of Enrollment | Number | participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Resolution of Diarrhea | To evaluate the safety and efficacy of CASAD added to the standard-of-care for the therapy of Clostridium difficile infection (C. difficile). | The study was terminated early due to slow enrollment. Of the 2 patients enrolled, one took less than 50% of the prescribed study drug. The results are not evaluable. | Posted | 42 days |
|
| |||||||||||||||||||
| Secondary | Stools Per Day | Compare the number of liquid stools per day during treatment period | The study was terminated early due to slow enrollment. One of the two patients enrolled took less than 50% of the prescribed study drug. | Posted | 14 days |
|
| |||||||||||||||||||
| Secondary | Resolution of Abdominal Pain | Compare time to resolution of abdominal pain | The study was terminated early due to slow enrollment. One of the two patients enrolled took less than 50% of the prescribed study drug. | Posted | 14 days |
|
| |||||||||||||||||||
| Secondary | Absence of Relapse | Compare sustained clinical response | The study was terminated early due to slow enrollment. One of the two patients enrolled took less than 50% of the prescribed study drug. | Posted | 42 days |
|
| |||||||||||||||||||
| Secondary | Side-effects and Complications | Compare side-effects and complications | The study was terminated early due to slow enrollment. One of the two patients enrolled took less than 50% of the prescribed study drug. | Posted | 42 days |
|
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Adverse events were collected during active study period of 6 weeks.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Open Label CASAD | Treatment with CASAD for 14 days | 0 | 2 | 2 | 2 |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Nausea | Gastrointestinal disorders | Non-systematic Assessment | unrelated to study drug, patient recovered with no residual effect. |
| |
| Bloating | Gastrointestinal disorders | Non-systematic Assessment | probably related to study drug, patient recovered, no action taken |
| |
| Burping/Gas | Gastrointestinal disorders | Non-systematic Assessment | Possible relationship to study drug, no action taken, patient recovered |
| |
| Dark urine | Renal and urinary disorders | Non-systematic Assessment | No action taken, patient recovered with no residual effects |
|
This study was terminated early for slow enrollment. Only 2 patients were enrolled during the open period. One of the two took less than 50% of the prescribed study drug. The results are not meaningful.
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Richard scruggs | Salient Pharmaceuticals Incorporated | 7135899859 | rscruggs@salientpharmaceuticals.com |
| ID | Term |
|---|---|
| D003967 | Diarrhea |
| D007239 | Infections |
| D013035 | Spasm |
| ID | Term |
|---|---|
| D012817 | Signs and Symptoms, Digestive |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D020879 | Neuromuscular Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D000077250 | Calcium Aluminosilicate |
| ID | Term |
|---|---|
| D000538 | Aluminum Silicates |
| D000537 | Aluminum Oxide |
| D017607 | Aluminum Compounds |
| D007287 | Inorganic Chemicals |
| D017640 | Silicates |
| D008903 | Minerals |
| D010087 | Oxides |
| D017601 | Oxygen Compounds |
| D012824 | Silicic Acid |
| D012822 | Silicon Dioxide |
| D017655 | Silicon Compounds |
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