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D004927: Escherichia coli Infections

Developed by Shray Alag, The Harker School
Sections: Correlations, Clinical Trials, and HPO

Correlations computed by analyzing all clinical trials.

Navigate: Clinical Trials and HPO


Correlated Drug Terms (7)


Name (Synonyms) Correlation
drug2235 Ivermectin 3mg Tab Wiki 1.00
drug5245 strain CVD 1208S-122 Wiki 1.00
drug1982 Hydroxychloroquine Sulfate Tablets Wiki 0.71
Name (Synonyms) Correlation
drug3335 Povidone-Iodine Wiki 0.50
drug4781 Zinc Wiki 0.35
drug4690 Vitamin C Wiki 0.27
drug3195 Placebo Wiki 0.04

Correlated MeSH Terms (3)


Name (Synonyms) Correlation
D004405 Dysentery, Bacillary NIH 1.00
D003141 Communicable Diseases NIH 0.07
D007239 Infection NIH 0.05

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002740 Recurrent E. coli infections HPO 1.00

Clinical Trials

Navigate: Correlations   HPO

There is one clinical trial.


1 Phase 1 Study of the Safety, Tolerability, and Immunogenicity of Oral Doses of CVD 1208S-122, a Prototype Attenuated Shigella Flexneri 2a Live Vector Expressing Enterotoxigenic Escherichia Coli Antigens

The purpose of this study is to determine whether a live, oral, combined Shigella-ETEC vaccine candidate, known as strain CVD 1208S-122, is safe and immunogenic.

NCT04634513
Conditions
  1. Shigella Infection
  2. Enterotoxigenic Escherichia Coli Infection
Interventions
  1. Biological: strain CVD 1208S-122
  2. Other: Placebo
MeSH:Infection Communicable Diseases Dysentery, Bacillary Escherichia coli Infections
HPO:Recurrent E. coli infections

Primary Outcomes

Description: The number, proportion, and severity of fever, diarrhea, or dysentery (hemoccult testing will only be performed during the inpatient days) within 7 days of vaccination, for all those receiving vaccine and for each of the vaccine dosages evaluated

Measure: Number, Proportion, and Severity of Fever, Diarrhea, or Dysentery

Time: 7 days following vaccination

Description: The number, proportion, and severity of solicited local and systemic adverse reactions (diarrhea, dysentery, fever, nausea, vomiting, abdominal discomfort, tenesmus, myalgia, arthralgia, and anorexia) within 7 days of vaccination for all those receiving vaccine and for each of the vaccine dosages evaluated

Measure: Number, Proportion, and Severity of Solicited Local and Systemic Adverse Reactions

Time: 7 days following vaccination

Description: The number, proportion, severity, and relatedness of non-serious unsolicited adverse reactions within 28 days of vaccination for all those receiving vaccine and for each of the vaccine dosages evaluated

Measure: Number, Proportion, Severity, and Relatedness of Non-Serious Unsolicited Adverse Reactions

Time: 28 days following vaccination

Description: The number, proportion, and severity of clinical safety laboratory adverse events from the time of each study vaccination through approximately 7 days after each study vaccination.

Measure: Number, Proportion, and Severity of Clinical Safety Laboratory Adverse Events

Time: 7 days following vaccination

Description: The occurrence of SUSARs in the study

Measure: Occurrence of SUSARs

Time: The entire study period (6-7 months)

Description: The occurrence of all SAEs, regardless of the assessment of relatedness, from the time of the first vaccination through approximately 6 months after the last study vaccination

Measure: Occurrence of all SAEs

Time: The entire study period (6-7 months)

Description: The geometric mean number (and interquartile range) of vaccine organisms, per day and at the peak of shedding, expressed as cfu/mL for each dosage group

Measure: Geometric Mean Number of Vaccine Organisms

Time: for each day of the 7 days following vaccination

Description: The number and proportion of sequential days of fecal shedding of Shigella organisms which are documented to contain the genes expressing ETEC antigens for each dosage group. Genetically stable organisms will be defined as being PCR positive for Shigella (ipaH or virG), CFA/I (cfaB), and LTB (eltB)

Measure: Number and Proportion of Sequential Days of Fecal Shedding of Shigella Organisms

Time: for each day of the 7 days following vaccination

HPO Nodes


HPO

Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials


HPO Nodes


Reports

Data processed on December 13, 2020.

An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

Drug Reports   MeSH Reports   HPO Reports  

Interventions

4,818 reports on interventions/drugs

MeSH

706 reports on MeSH terms

HPO

306 reports on HPO terms

All Terms

Alphabetical index of all Terms

Google Colab

Python example via Google Colab Notebook