- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04477889
Methodist Health System COVID-19 Patient Registry
May 15, 2026 updated by: Methodist Health System
This is a prospective cohort observational registry study that will include data on all patients who are treated at MHS facilities for COVID-19.
Study Overview
Detailed Description
This is a prospective cohort observational registry study that will include data on all patients who are treated at MHS facilities for COVID-19.
Data including, but not limited to demographics, comorbidities, medications, treatment, and clinical outcomes will be collected from February 2020 to December 2025.
Subjects will undergo no additional tests or procedures as part of this registry study.
All patient data will be obtained from the patient's electronic health records (EHR) of the hospital or clinic in a retrospective manner.
The process for gathering the data will not influence treatment decisions.
There will be no direct patient contact associated with inclusion in this registry study.
Study Type
Observational
Enrollment (Actual)
550
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
-
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Texas
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Dallas, Texas, United States, 75203
- Clinical Research Institute Methodist Health System
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
All adult patients who are treated at MHS facilities for COVID-19.
Description
Inclusion Criteria:
- Patient tested positive for COVID-19 (SARS-CoV-2)
- Patient sought care for COVID-19 at a MHS facility
- Aged 18 years or older
Exclusion Criteria:
- Patient that do not have COVID-19
- Non-confirmed COVID-19 patients
- Aged 17 years or younger
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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COVID-19 Cohort
Patients treated at MHS facilites for COVID-19
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Patients treated for COVID-19
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Synopsis for COVID Bariatric, Hepato-Biliary and Colorectal surgery study
30 Day Mortality after surgery in patients with COVID19 infection who undergo elective bariatric, hepato-biliary and colorectal surgery.
|
Patients treated for COVID-19
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Characteristics
Time Frame: June 2020 - Dec 2025
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Patient characteristics
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June 2020 - Dec 2025
|
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Treatment Measures and Intervention strategies
Time Frame: June 2020 - Dec 2025
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Treatment measures and intervention strategies
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June 2020 - Dec 2025
|
|
Clinical and survival outcomes
Time Frame: June 2020 - Dec 2025
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Clinical and survival outcomes
|
June 2020 - Dec 2025
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Crystee Cooper, DHEd, Methodist Health System
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)
June 20, 2020
Primary Completion (Actual)
June 16, 2025
Study Completion (Actual)
June 16, 2025
Study Registration Dates
First Submitted
July 17, 2020
First Submitted That Met QC Criteria
July 17, 2020
First Posted (Actual)
July 20, 2020
Study Record Updates
Last Update Posted (Actual)
May 19, 2026
Last Update Submitted That Met QC Criteria
May 15, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 024.CRI.2020.A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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