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Diarrhea clinical trials

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NCT ID: NCT00682955 Completed - Clinical trials for Incidence of Acute Diarrhea

Comparing the Efficacy of Different Zinc Formulations in the Treatment of Diarrhea

Zinc
Start date: August 2007
Phase: N/A
Study type: Interventional

This project is aimed to evaluate the efficacy of two different zinc formulations (dispersible Zinc tablets versus Zinc suspension) for the treatment of acute diarrhea in hospital based settings. Additionally we intend to compare the effectiveness of treatments of different groups on the basis of usage of Zinc in the treatment of diarrhoea, and to monitor additional treatment components such as ORS, antibiotic usage rates.

NCT ID: NCT00658151 Not yet recruiting - Clinical trials for Antibiotic-Associated Diarrhea

Ultrasound Diagnosis of Antibiotic Associated Diarrhea

Start date: April 2008
Phase: N/A
Study type: Observational

The hypothesis is that there are unique sonographic characteristics of antibiotic-associated diarrhea. We will compare the ultrasound findings in patients who received antibiotics and developed diarrhea to toxin analysis for clostridium difficile in stool in order to find differences in the sonographic findings in the positive and negative cases.

NCT ID: NCT00650637 Terminated - Diarrhea Clinical Trials

A Study to Determine Effective Prophylaxis and Treatment of Nelfinavir-Associated Diarrhea

Start date: January 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine the efficacy and safety of calcium carbonate for the prevention of nelfinavir-associated diarrhea and to evaluate the efficacy and safety of calcium carbonate in combination with loperamide for the treatment of nelfinavir-associated diarrhea.

NCT ID: NCT00641199 Completed - Clinical trials for Antibiotic-Associated Diarrhea

Probiotics for Prevention of Antibiotic-associated Diarrhea

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if ingestion of a probiotic formula (Jarrow-Dophilus EPS)reduces incidence of diarrhea and improves the quality of life of patients receiving antibiotic therapy.

NCT ID: NCT00624975 Terminated - Diarrhea Clinical Trials

Safety and Immunogenicity of Peru-15 Vaccine When Given With Measles Vaccine in Healthy Indian and Bangladeshi Infants

Start date: November 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to confirm the safety and immunogenicity of Peru-15 vaccine in infants when given simultaneously with measles vaccine.

NCT ID: NCT00619125 Completed - Clinical trials for IBS, Diarrhea Predominant

Proposal Evaluating Time-specific Relationships Between Variables of Pain, Stress, and Bloating in IBS Diarrhea and Constipation Symptoms Using a Palm Pilot

Start date: April 2008
Phase: N/A
Study type: Observational

Purpose: The associations between pain, stress, bloating, and their short interval temporal relationships to defecation in IBS D, C & M are of great interest to the field of functional GI disorders, but have not been adequately studied. Broad recall based assessments (i.e.,over past week or month) of pain and bloating have been key features of the diagnosis of IBS, however such long term retrospective recall of symptom experience has been shown to be unreliable and influenced by outside factors (heuristics, recall bias, etc.). Short interval assessment may provide a more accurate picture of patient symptom experience Participants: Patients with IBS in general and IBS subtypes (IBS-C, D, M) Procedures (methods): Study participants could be asked to record data at randomly assigned points throughout the day, as well as during the course of a diarrheal or constipated stool (i.e., prior to and right after a bowel movement).

NCT ID: NCT00616200 Completed - Clinical trials for Diarrhea Predominant Irritable Bowel Syndrome

Effects of a Very Low Carbohydrate Diet on Symptoms of Irritable Bowel Syndrome (IBS)

Start date: August 2009
Phase: N/A
Study type: Interventional

The purposes of this study are to prospectively determine the effect of a very low carbohydrate diet on quality of life and gastrointestinal symptoms in patients with diarrhea-predominant irritable bowel syndrome (IBS-D); and to determine possible physiological correlates of symptom improvement, as related to post-prandial 5-hydroxytryptamine (5-HT) release, weight loss and fiber content.

NCT ID: NCT00591357 Suspended - Clinical trials for Clostridium Difficile

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

loperamide
Start date: October 2007
Phase: Phase 4
Study type: Interventional

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.

NCT ID: NCT00589771 Completed - Clinical trials for Diarrhea Dominant Irritable Bowel Syndrome

Saccharomyces Boulardii in Irritable Bowel Syndrome

SB-IBS
Start date: January 2010
Phase: Phase 3
Study type: Interventional

Various studies have been conducted in past using different strains of probiotics in evaluating IBS symptoms. The results are by no means consistent and the overall impact of probiotics in IBS remains unclear. However, recently O'Mahony L et al have shown that Bifidobacterium infantis 35624 alleviates symptoms in IBS; this symptomatic response was associated with normalization of the ratio of an anti-inflammatory to a proinflammatory cytokine (IL-10/IL-12 ratio), suggesting an immune-modulating role for this organism, in this disorder.Saccharomyces boulardii is a probiotic yeast that has been successfully used for the antibiotic induced diarrhea, prevent relapse of Clostridium difficile and Crohn's disease. It ameliorates intestinal injury and inflammation caused by a wide variety of enteric pathogens.We therefore plan a Double-blind, randomized, placebo-controlled study to assess the effects of Saccharomyces boulardii in improving symptomatology of diarrhea predominant IBS and its effect on quality of life. We also plan to assess the changes in the relative production of anti-inflammatory interleukin (IL)-10 to proinflammatory cytokines (IL-12, IL-8 and TNFα).

NCT ID: NCT00582426 Completed - Clinical trials for Chemotherapy-induced Diarrhea

Evaluation of Octreotide LAR in Prevention of Chemotherapy-induced Diarrhea

LARCID
Start date: April 2008
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy of Octreotide LAR in preventing chemotherapy-induced diarrhea (with regimens that contain 5 fluorouracil, irinotecan and capecitabine)in patients with colorectal cancer.