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

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.

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

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

  1. 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.

Clinical Trials on Immune System Diseases

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