COVID
Conditions
Brief summary
It is a randomized controlled trial to assess the efficacy of Ivermectin in COVID-19. Patient recruited will be assigned to two groups one group will be given ivermectin with standard chloroquine regimen and the other group will be receiving chloroquine only. Out come will be recorded by documenting PCR reports at 48, 96 and 144 hours.
Detailed description
INTERVENTION It will be a randomized controlled trial which will be done on COVID-19 patients proven by PCR fulfilling the criteria (asymptomatic/mild to moderate severity). They will be divided into two groups after randomization. Group A will be administered Ivermectin single dose of 12grams along with Chloroquine as per existing hospital guidelines and group B will be given Chloroquine alone. Dose of Ivermectin to be repeated at 1 week if PCR stays negative. PCR will be done on alternate days (48, 96 and 144hours) and the duration at which the PCR becomes negative will be compared. Dose of drug subject to change in accordance with patient response or possible side effect. ELIGIBILITY CRITERIA INCLUSION CRITERIA In order to be eligible to participate in this study, an individual must meet all of the following criteria: Provision of signed and dated informed consent form Stated willingness to comply with all study procedures and availability for the duration of the study Male or female, aged 15 to 65 years In good general health with no or mild symptoms of Corona virus disease PCR positive for SARS-Cov-2. Ability to take oral medication and be willing to adhere to the drug intake regimen EXCLUSION CRITERIA An individual who meets any of the following criteria will be excluded from participation in this study: Severe symptoms likely attributed to Cytokine Release Storm. Malignant diseases, diabetes mellitus, chronic kidney disease and cirrhosis liver with CPT class B or C.
Interventions
12 mg single dose of Ivermectin will be given to intervention arm
Sponsors
Combined Military Hospital, Pakistan
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
15 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Male or female, aged 15 to 65 years * In good general health with no or mild to moderate symptoms of Corona virus disease * PCR positive for SARS-Cov-2. * Ability to take oral medication and be willing to adhere to the drug intake regimen
Exclusion criteria
* Severe symptoms likely attributed to Cytokine Release Storm. * Malignant diseases, diabetes mellitus, chronic kidney disease and cirrhosis liver with CPT class B or C.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Negative PCR | 144 hours | PCR will be done at 48, 96 and 144 hours |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Need for mechanical ventilation | 4 weeks | All patients will be assessed for requirement of mechanical ventilation in both the groups |
Countries
Pakistan
Contacts
Primary ContactAsma Asghar, FCPS MED
Backup ContactNajma Parveen, FCPS med
Outcome results
None listed