CASAD for Severe Diarrhea in the Emergency Department

Stopped early · Not applicable · Has a placebo group

Conditions studied: Cancer, Diarrhea

In brief

The goal of this clinical research study is to learn if calcium alumina-silicate (CASAD) can help to stop your diarrhea. Researchers also want to know if this drug can help decrease the duration of your diarrhea. In this study, CASAD will be compared to a placebo. A placebo is not a drug. It looks like the study drug but it is not designed to treat any disease or illness. It is designed in this study to be compared with the study drug to learn if the study drug has any real effect.

Key facts

Study ID

NCT02018653

Run by

M.D. Anderson Cancer Center

People needed

2

Starts

2013-12-01

Expected to finish

2014-08-01

Last updated by the study team

2018-07-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Cancer patients presenting to the EC or an acute care clinic for NCI grade >/= 2 diarrhea
• Able to understand the description of the study and give informed consent
• Patients must be willing to and capable of providing frequent assessments for the duration of the study
• English-speaking

You may not qualify if…

• Patients will not be approached while they have : a) evidence of fever or severe abdominal pain, melena, overt blood in stool; b) any clinical suspicion or evidence of peritonitis or bowel perforation; c) s/p allogenic stem cell transplant
• Patients will not be approached if the EC physician thinks that the diarrhea is due to Crohn's disease, ulcerative colitis, Celiac disease, graft-versus-host disease, short-gut syndrome, neuroendocrine paraneoplastic syndromes (e.g., MEN, VIPomas, etc.), or malabsorption syndromes
• Patients who are status post stem cell transplantation (both autologous or allogenic)
• Patients who are status post immunotherapy (including those who are receiving or have received ipilimumab)
• Patients participating in other clinical trials for diarrhea
• Patients with a known allergy to any components of the CASAD formulation
• Patients whose current medication schedule would not permit an approximate 2 hour window between administration of CASAD and other scheduled medications
• Patients who cannot comply with medications
• Patients taking any clay products
• Patients with radiological evidence of megacolon, intraperitoneal free air, pneumatosis intestinalis, or fecal impaction
• History of significant neurological or psychiatric disorders that would impede giving consent, treatment, or follow up
• Patients who are pregnant
• Patients less than 18 years of age

Where it is running

• University of Texas MD Anderson Cancer Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

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