IRCT20200718048129N1RecruitingPhase 3
Evaluation and comparison of the effectiveness of Hydroxychloroquin versus Clarithromycin in recovery of dyspnea and Caugh at the end of the acute phase of COVID-19 treatment
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Enrollment
- 45
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 20 years to 50 years (—)
- Sex
- All
Inclusion Criteria
- •Patients with definitive diagnosis of COVID19 were hospitalized and treated
- •Patients with COVID19 who still have dyspena and cough two weeks after discharge from the hospital
- •Patients with COVID19 who continue to have lung involvement on CT SCAN two weeks after discharge
Exclusion Criteria
- •Patients with comorbidities such as chronic heart or lung disease before COVID19
- •The need for long-term use of drugs that have an irreversible interaction with the drugs used in the plan.
Investigators
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