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Last Updated: October 18, 2019

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CLINICAL TRIALS PROFILE FOR IMODIUM MULTI-SYMPTOM RELIEF

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Clinical Trials for Imodium Multi-symptom Relief

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00075868 Octreotide in Preventing or Reducing Diarrhea in Patients Receiving Chemoradiotherapy for Anal or Rectal Cancer Completed National Cancer Institute (NCI) Phase 3 2003-12-01 RATIONALE: Octreotide may be effective in preventing or controlling diarrhea in patients who are undergoing chemoradiotherapy for anal or rectal cancer. It is not yet known whether octreotide is effective in treating diarrhea. PURPOSE: This randomized phase III trial is studying octreotide in preventing or reducing diarrhea in patients who are undergoing chemoradiotherapy for anal or rectal cancer.
NCT00075868 Octreotide in Preventing or Reducing Diarrhea in Patients Receiving Chemoradiotherapy for Anal or Rectal Cancer Completed Radiation Therapy Oncology Group Phase 3 2003-12-01 RATIONALE: Octreotide may be effective in preventing or controlling diarrhea in patients who are undergoing chemoradiotherapy for anal or rectal cancer. It is not yet known whether octreotide is effective in treating diarrhea. PURPOSE: This randomized phase III trial is studying octreotide in preventing or reducing diarrhea in patients who are undergoing chemoradiotherapy for anal or rectal cancer.
NCT00292344 Rifaximin, Loperamide and the Combination to Treat Travelers' Diarrhea Completed Valeant Pharmaceuticals International, Inc. Phase 4 2004-06-01 Most cases of travelers' diarrhea are caused by bacterial pathogens which respond slowly to antibiotic treatment.The study was designed to determine the value of rapidly acting loperamide (imodium) combined with curative dose of the poorly absorbed rifaximin in travelers' diarreha treatment.
NCT00292344 Rifaximin, Loperamide and the Combination to Treat Travelers' Diarrhea Completed The University of Texas Health Science Center, Houston Phase 4 2004-06-01 Most cases of travelers' diarrhea are caused by bacterial pathogens which respond slowly to antibiotic treatment.The study was designed to determine the value of rapidly acting loperamide (imodium) combined with curative dose of the poorly absorbed rifaximin in travelers' diarreha treatment.
NCT00360828 Phase II Study of Irinotecan HCI for Recurrent Anaplastic Astrocytomas, Mixed Malignant Gliomas, and Oligodendrogliomas Terminated H. Lee Moffitt Cancer Center and Research Institute Phase 2 2006-02-01 Phase 2 trial to explore the efficacy and safety of irinotecan (CPT-11). Also administered at each cycle was zofran/Kytril/Anzemet, decadron, and IV atropine. At each cycle, patient exams and interviews as well as lab results were to help the research team to determine the symptomatic side effects of the treatment. Recorded past toxicities were to be compared with current side effects.
NCT00583531 Safety and Efficacy of AST-120 in the Treatment of Antibiotic-Refractory Pouchitis Terminated Ocera Therapeutics Phase 2 2007-03-01 This is an open-label pilot study in which all patients will receive AST-120 for 4 weeks. Patients will discontinue antibiotics at study entry. They may continue other previously prescribed treatments (e.g., probiotics and/or nutritional agents) at the discretion of the study doctor. The purpose of the study is to assess whether the investigational medication AST-120 will be a safe and effective treatment for the symptoms of pouchitis, a chronic inflammatory condition, in patients whose symptoms have not responded well to antibiotics. An initial group of 10 patients will be enrolled. If there are no serious side effects associated with the study drug and at least 3 of the 10 patients respond, a second group of 10 patients may be enrolled. Patients will have clinic visits at the start of the study and at week 4. Patients will be checked by phone on a weekly basis for symptom response, compliance and development of side effects. Endoscopies will be performed at the start of the study and at week 4 or early termination.
NCT00591357 Efficacy of Loperamide for C. Difficile Colitis and Other Diarrheal Diseases Associated With Antibiotic Therapy Suspended VA Medical Center, Houston Phase 4 2007-10-01 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.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Imodium Multi-symptom Relief

Condition Name

Condition Name for Imodium Multi-symptom Relief
Intervention Trials
Diarrhea 4
Fecal Incontinence 3
Travelers' Diarrhea 2
Malignant Neoplasms of Urinary Tract 1
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Condition MeSH

Condition MeSH for Imodium Multi-symptom Relief
Intervention Trials
Diarrhea 8
Fecal Incontinence 3
Dysentery 2
Rectal Neoplasms 2
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Clinical Trial Locations for Imodium Multi-symptom Relief

Trials by Country

Trials by Country for Imodium Multi-symptom Relief
Location Trials
United States 57
Mexico 6
United Kingdom 1
India 1
Kenya 1
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Trials by US State

Trials by US State for Imodium Multi-symptom Relief
Location Trials
Texas 6
North Carolina 4
California 3
Missouri 2
Alabama 2
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Clinical Trial Progress for Imodium Multi-symptom Relief

Clinical Trial Phase

Clinical Trial Phase for Imodium Multi-symptom Relief
Clinical Trial Phase Trials
Phase 4 6
Phase 3 3
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Imodium Multi-symptom Relief
Clinical Trial Phase Trials
Completed 8
Terminated 5
Not yet recruiting 2
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Clinical Trial Sponsors for Imodium Multi-symptom Relief

Sponsor Name

Sponsor Name for Imodium Multi-symptom Relief
Sponsor Trials
M.D. Anderson Cancer Center 3
Johnson & Johnson Consumer and Personal Products Worldwide 2
The Cleveland Clinic 1
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Sponsor Type

Sponsor Type for Imodium Multi-symptom Relief
Sponsor Trials
Other 24
Industry 13
NIH 4
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