- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04974177
A Study to Determine the Role of Physician Gestalt in Predicting COVID-19 in Patients
March 10, 2024 updated by: SARASWATHY M, Jubilee Mission Medical College and Research Institute
A Prospective Observational Study to Determine the Role of Physician Gestalt in Clinical Prediction of COVID-19
THIS IS A PROSPECTIVE OBSERVATIONAL STUDY TO DETERMINE THE ROLE OF PHYSICIAN GESTALT IN CLINICAL PREDICTION OF COVID 19.
Study Overview
Status
Completed
Detailed Description
Among patients attending the Emergency Department, prompt identification of possible cases of COVID 19 is important to avoid the spread.
An immediate clinical diagnosis is important for point of care decision making on choice of treatment facility as well as for triaging, testing and to quarantine patients admitted to the hospital from emergency room.
Hence this study attempts to find out the role of physician gestalt in early diagnosis and differentiation of COVID 19.
Study Type
Observational
Enrollment (Actual)
876
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Kerala
-
Thrissur, Kerala, India, 680005
- Jubilee Mission Medical College
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
All patients presenting to ED, who undergo COVID 19 specific testing.
Description
Inclusion Criteria:
- All patients presenting to ED, who undergo COVID 19 specific testing.
Exclusion Criteria:
- Patients with active COVID 19 disease diagnosed outside All brought dead cases. All patients not consenting to take part in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Sensitivity, specificity, positive and negative likelihood ratio of physician gestalt in diagnosis of COVID 19 in patients presenting to ED who are being sent for COVID 19 specific testing.
Time Frame: march 2021- september 2022
|
march 2021- september 2022
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Sensitivity, specificity, positive and negative likelihood ratio of clinical and epidemiological variables in patients presenting to ED who are being sent for COVID 19 specific testing.
Time Frame: march 2021- september 2022
|
march 2021- september 2022
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 15, 2021
Primary Completion (Actual)
September 15, 2022
Study Completion (Actual)
September 15, 2022
Study Registration Dates
First Submitted
July 21, 2021
First Submitted That Met QC Criteria
July 21, 2021
First Posted (Actual)
July 23, 2021
Study Record Updates
Last Update Posted (Actual)
March 13, 2024
Last Update Submitted That Met QC Criteria
March 10, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 13/21/IEC/JMMC&RI
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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