Evaluation of a Diagnostic Enteric Card for Management of Diarrhea
NCT ID: NCT00736567
Last Updated: 2014-10-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
436 participants
OBSERVATIONAL
2008-05-31
2009-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Point-of-Use Pathogen Identification Tool for Diarrhea
NCT03394040
Multidrug Resistant Shigella Infection in Bangladesh
NCT03778125
Relationship Between C. Difficile Toxins' Serum Level With C. Difficile Infection
NCT03586206
Probiotics Administration Via Colonoscopic Spray and Oral Administration in CDAD Patients
NCT05770726
C. Difficile Toxin Levels in Stool From Healthy Individuals Following Standard of Care Antibiotic Treatment for CDI.
NCT07250724
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Provide written informed consent from at least one parent in the case of children under 18 years of age.
* Provide written informed consent for those participants above 18 years of age.
* Provide assent in the case of children 10 years of age or greater.
Exclusion Criteria
* Parents are unwilling or unable to provide written informed consent.
* Report using antibiotics in the last 30 days.
* Adolescent (\<18 years old) parent of a child already enrolled in the study.
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universidade Federal do Ceara
OTHER
University of Virginia
OTHER
Micronics, Inc.
INDUSTRY
Washington University Early Recognition Center
OTHER
PATH
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital Infantil Albert Sabin
Fortaleza, CearĂ¡, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
07-0008
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.