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D003139: Common Cold

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 (4)


Name (Synonyms) Correlation
drug814 Coldamaris pro, nasal spray Wiki 0.71
drug3171 Standard Donor Plasma Wiki 0.71
drug884 Convalescent Plasma Wiki 0.27
Name (Synonyms) Correlation
drug2985 Saline Wiki 0.22

Correlated MeSH Terms (9)


Name (Synonyms) Correlation
D029424 Pulmonary Disease, Chronic Obstructive NIH 0.27
D008173 Lung Diseases, Obstructive NIH 0.25
D012141 Respiratory Tract Infections NIH 0.12
Name (Synonyms) Correlation
D014777 Virus Diseases NIH 0.07
D007239 Infection NIH 0.06
D045169 Severe Acute Respiratory Syndrome NIH 0.06
D003141 Communicable Diseases NIH 0.05
D018352 Coronavirus Infections NIH 0.05
D011014 Pneumonia NIH 0.04

Correlated HPO Terms (3)


Name (Synonyms) Correlation
HP:0006510 Chronic pulmonary obstruction HPO 0.29
HP:0006536 Pulmonary obstruction HPO 0.27
HP:0011947 Respiratory tract infection HPO 0.12

Clinical Trials

Navigate: Correlations   HPO

There are 2 clinical trials


1 Audio Data Collection for Identification and Classification of Coughing

An open access study that will define and collect digital measures of coughing in multiple populations and public spaces using various means of audio data collection.

NCT04326309
Conditions
  1. COVID-19
  2. Coronavirus Infections
  3. Hay Fever
  4. Asthma
  5. Chronic Obstructive Pulmonary Disease
  6. Influenza
  7. Common Cold
  8. Respiratory Tract Infections
  9. Healthy
MeSH:Infection Communicable Diseases Respiratory Tract Infections Coronavirus Infections Severe Acute Respiratory Syndrome Common Cold Lung Diseases, Obstructive Pulmonary Disease, Chronic Obstructive
HPO:Chronic pulmonary obstruction Pulmonary obstruction Respiratory tract infection

Primary Outcomes

Description: Size of collected audio dataset measured as number of collected cough sounds, targeting ≥10,000 identified coughs.

Measure: Dataset size

Time: 14 days

Secondary Outcomes

Description: Identification of cough sounds by the existing mathematical model with ≥ 99% specificity and ≥ 60% sensitivity

Measure: Cough sound identification

Time: 14 days

Description: Increase in the sensitivity of the mathematical model to cough sounds to ≥ 70% while retaining the specificity of ≥ 99%

Measure: Improvement of the existing model

Time: 14 days

Description: Determination of the level of acceptance and satisfaction of the solution by patients by means of a Standard Usability Questionnaire to provide feedback. The score ranges from 10 to 50, higher score indicating a better usability.

Measure: Evaluate the usability of the application

Time: 14 days
2 Clinical Trial to Evaluate the Efficacy of an Iota-Carrageenan Nasal Spray to Reduce Symptoms Caused by SARS-CoV-2 and Other Respiratory Viruses in Healthcare Workers Managing COVID-19 Patients

This is a prospective, randomized placebo-controlled double blinded clinical trial in frontline healthcare workers managing COVID-19 patients. Participants will be weekly tested for SARS-CoV-2 and a panel of respiratory viruses. Treatment will be 3times a day for 84 days one puff into each nostirl and 3 puffs into mouth. Daily a symptom score will be recorded. The primary objective of the trial is to demonstrate that prophylactic treatment of health care workers managing COVID-19 patients with iota-carrageenan reduces symptoms of SARS-CoV-2 infections as well as infections with other respiratory viruses when compared to a placebo-treated control group.

NCT04681001
Conditions
  1. Respiratory Viral Infection
  2. Common Cold
  3. Severe Acute Respiratory Syndrome (SARS) Pneumonia
  4. COVID-19
  5. Corona Virus Disease
Interventions
  1. Device: Coldamaris pro, nasal spray
MeSH:Infection Virus Diseases Severe Acute Respiratory Syndrome Coronavirus Infections Common Cold Pneumonia
HPO:Pneumonia

Primary Outcomes

Description: daily assessment of subjective COVID-19 symptom score

Measure: Presence of COVID-19 symptoms including symptoms of respiratory viral infection documented in a diary

Time: 84 days

Secondary Outcomes

Description: weekly assessment of SARS-CoV-2, Influenza A, Human Metapneumovirus, Influenza A - subtype H1, Adenovirus, Influenza A - subtype H3, Parainfluenza 1, Influenza A - subtype 2009 H1N1, Parainfluenza 2, Influenza B, Parainfluenza 3, Parainfluenza 4, Coronavirus HKU1, Respiratory Syncytial Virus A, Coronavirus N63L, Respiratory Syncytial Virus B, Coronavirus OC43, Rhinovirus/Enterovirus, Coronavirus 229E, Human Bocavirus, Chlamydophila pneumoniae, Mycoplasma pneumoniae, Legionella pneumophila

Measure: Nasal swabs for analysis of viruses by PCR

Time: 84 days

Description: beginn and end of trial

Measure: Serology of antibodies against SARS-CoV-2

Time: 84 days

Description: weekly nasal swabs for analysis of viruses

Measure: Number of viral co-infections dedected by PCR

Time: 84 days

HPO Nodes


HPO

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


HPO Nodes


Reports

Data processed on January 01, 2021.

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

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706 reports on MeSH terms

HPO

306 reports on HPO terms

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