Observational Study on the Use of Ivermectin as an Outpatient Treatment Option for COVID-19
Purpose
Ivermectin is currently being utilized by a number of physicians in the local area. My objective will be to enroll these patients at the time of their evaluation for COVID-19 infection and to follow their progress through their recovery.
Conditions
- Covid19
- COVID-19 Pneumonia
- COVID-19 Respiratory Infection
- COVID-19 Acute Bronchitis
Eligibility
- Eligible Ages
- Between 12 Years and 110 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Between the ages of 12-110 years old - Has a recently completed COVID test - Symptomatic and seeking treatment - Willingness to participate and have follow-up - Able and willing to take medications and treatment suggestions from the physician
Exclusion Criteria
Lack of symptoms, uncertain of COVID-19 status, outside of age limits for treatment - No recent COVID test results - Asymptomatic, even if COVID positive - Outside of acceptable age range - Meets criteria for hospital admission - Unwilling to participate in trial study or have follow-up
Study Design
- Phase
- Study Type
- Observational [Patient Registry]
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
Arm | Description | Assigned Intervention |
---|---|---|
COVID-19 patients treated with Ivermectin | This group of patients will be those who requested to be treated with Ivermectin and whom have been prescribed such by different physicians. This group may or may not include those treated with Monoclonal Antibodies or Remdesivir. |
|
COVID-19 patients declining Ivermectin and wanting traditional treatment | This group of patients will be those who do not request to be treated with Ivermerctin and who want to be treated with a more traditional, minimalist approach. This group may or may not include those treated with Monoclonal Antibodies or Remdesivir. |
|
Recruiting Locations
San Antonio, Florida 33576
More Details
- NCT ID
- NCT05045937
- Status
- Unknown status
- Sponsor
- Patrick Robinson
Detailed Description
Patients at local physician clinics as well as my own clinic will be enrolled at the time they are evaluated for having COVID-19. Patients enrollment will be voluntary and based upon their request for treatment with Ivermectin. These patients will be questioned on symptoms and the timing of those symptoms in detail. They will then be followed throughout their treatment course to evaluate their recovery experience. Detailed accounts of their symptoms and their resolution will be followed. The study patients will stop being followed when they are either admitted to the hospital or are deemed to be symptom free. Any other medications prescribed to the patients will also be tracked. Medical histories will be taken and documented to make comparisons at the end of the study. Those patients not requesting Ivermectin will also be followed for comparisons at a later date.