Recovering Damaged Cells for Sequelae Caused by COVID-19, SARS-CoV-2 (NCT04846010) | Clinical Trial Compass
UnknownPhase 1/2
Recovering Damaged Cells for Sequelae Caused by COVID-19, SARS-CoV-2
United States2,000 participantsStarted 2021-03-01
Plain-language summary
Post-acute sequelae of SARS-CoV-2 infection can cause multiple system function disorders, and complicated symptoms last for an extended period. The virus can cause this continued infection, or the virus causes immune system function disorder and post-infectious autoimmune disease. The clinical symptoms can be smell loss, taste loss to liver function disorder, kidney function failure, different. No matter how complicated the systems showed in the clinic, all of the symptoms are due to the specific cells being damaged. Our clinical study is focused on recovering the damaged structure and function of the cells that could restore the organ function back to normal or close to normal
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* The participants must receive medical herbs as a treatment method;
* Participants are not limited by age, sex, race, or location;
* Participants are including infants;
* Participants are including pregnant woman;
* The participants had an infection history of SARS-CoV-2 in past one month;
* The participants provide SARS-CoV-s diagnoses (Molecular or Antigen). Test was \*positive, now hold negative reports
* Participants hold reports of immune system medics, like immunoglobulin M (IgM), immunoglobulin G (IgG);
* Reports that is evidence of specific organ damaged, including assay reports or image reports
* Participants must agree to take medical herbs for at least 3 months as one course continually;
* Participants must agree to repeat the assay and image test to monitor the treatment results;
* Participants must report their Manifestations clearly to investigators;
* Participants must agree to continue the next course of the treatment after the evaluation if it is necessary;
* The treatment goal is to become symptom-free, and experiment assays went to normal
Exclusion Criteria:
* Participants don't want to take medical herbs;
* Participants have symptoms of sequelae but is not caused by SARS-CoV-2 (COVID-19);
* Participants have not symptoms after COVID-19 infection, no assays abnormal either;
* Participants don't want to repeat the experiment assays;
* Participants are in E.R. or ICU during the application or enrollment;
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.