- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06107348
COVID-19 Post-Vaccination Observation
October 26, 2023 updated by: Yang I. Pachankis, PhD
COVID-19 Post-Vaccination Observation on Immune Exhaustion
The study started after the second COVID-19 vaccination of the participant with blood spots appearing on the skin with severe arthritis.
The study continued to the third-dose full vaccination of the participant with the recombined COVID-19 vaccination and afterwards.
The study completed until intervention.
Study Overview
Status
Active, not recruiting
Study Type
Observational
Enrollment (Actual)
1
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
-
-
Chongqing
-
Chongqing, Chongqing, China, 402762
- Residential Address
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The study population is currently focused on Asians.
Description
All COVID-19 vaccinated are eligible for inclusion.
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 |
|---|
|
Immune Disorder
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Chemiluminescent Immunoassay for Human Immunodeficiency Virus
Time Frame: 7 months
|
7 months
|
|
Carcinoembryonic Antigen
Time Frame: 7 months
|
7 months
|
|
Alpha Fetoprotein
Time Frame: 7 months
|
7 months
|
|
Carbohydrate Antigen 19-9
Time Frame: 7 months
|
7 months
|
|
Mucin-16
Time Frame: 7 months
|
7 months
|
|
Cancer Antigen 15-3
Time Frame: 7 months
|
7 months
|
|
Prostate-Specific Antigen
Time Frame: 7 months
|
7 months
|
|
Leukocytes
Time Frame: 7 months
|
7 months
|
|
Leukocyte Percentage
Time Frame: 7 months
|
7 months
|
|
Cholesterol
Time Frame: 7 months
|
7 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Pachankis YI. Questions of COVID-19: Institutional Derogations of Global Health. Lambert Academic Publishing. 2023. ISBN: 978-6206153849.
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)
July 1, 2021
Primary Completion (Actual)
January 4, 2023
Study Completion (Estimated)
December 24, 2023
Study Registration Dates
First Submitted
October 26, 2023
First Submitted That Met QC Criteria
October 26, 2023
First Posted (Actual)
October 30, 2023
Study Record Updates
Last Update Posted (Actual)
October 30, 2023
Last Update Submitted That Met QC Criteria
October 26, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SARS-Immune-00
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Time Frame
The data will be available upon completion and will be kept for as long as the repository is available.
IPD Sharing Supporting Information Type
- CSR
Study Data/Documents
-
Individual Participant Data Set
Information identifier: 10.17605/OSF.IO/2MGJK
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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