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Procedure
RD-X19 for Post-COVID Syndrome (EB-PCC-01 Trial)
N/A
Waitlist Available
Research Sponsored by KNOWBio Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
History of confirmed diagnosis of SARS-CoV-2 infection or COVID-19 per section 9.4
Agrees to maintain current medications without the addition of any new medications for relief of signs and symptoms of PCC during the entire study period, and, if used, to report ALL such medications (including over the counter and home remedies) to the study staff
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 weeks
Awards & highlights
EB-PCC-01 Trial Summary
This trial involves 7 days of treatment, 2 times per day, with weekly televisits and follow up visits up to 5 weeks after.
Who is the study for?
Adults over 22 with long COVID symptoms for at least 2 months post-infection, who haven't taken new meds for these symptoms recently. They must not have other health issues that could explain their symptoms or prevent full participation, and agree to avoid pregnancy.Check my eligibility
What is being tested?
The RD-X19 device is being tested on people with long COVID to see if it helps reduce their symptoms like cough, fatigue, shortness of breath, and brain fog. Participants will use the device twice daily for a week and be monitored through clinic visits and calls.See study design
What are the potential side effects?
Potential side effects are not detailed in the provided information but may include discomfort from using the device or reactions specific to light exposure due to the nature of RD-X19 treatment.
EB-PCC-01 Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have had a confirmed case of COVID-19.
Select...
I agree not to start any new medications for my condition during the study and will report all medications I take.
Select...
My symptoms have lasted for at least 2 months, continuously or on and off.
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I do not have any uncontrolled chronic or acute diseases causing my symptoms.
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I agree to self-treat twice daily, 6 hours apart, during the treatment.
EB-PCC-01 Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Primary Symptom Improvement
Secondary outcome measures
Secondary Symptom Improvement
EB-PCC-01 Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: ActiveActive Control1 Intervention
Group II: ShamPlacebo Group1 Intervention
Find a Location
Who is running the clinical trial?
KNOWBio Inc.Lead Sponsor
1 Previous Clinical Trials
25 Total Patients Enrolled
NAMSAOTHER
45 Previous Clinical Trials
16,882 Total Patients Enrolled
EmitBio Inc.Lead Sponsor
3 Previous Clinical Trials
573 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
What is the current participant headcount for this experiment?
"Affirmative. Clinicaltrials.gov reveals that this experiment, which was first made available on October 30th 2023 is still actively looking for participants to enroll in the study. The scientific team needs at least 60 patients from 2 different sites."
Answered by AI
Are investigators presently searching for participants in this research project?
"Based on the information from clinicaltrials.gov, this research endeavour is actively enrolling participants. Its public profile was created on October 30th 2023 and last updated at that same date."
Answered by AI
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