IRCT20200509047364N3
Not yet recruiting
Phase 3
Evaluation of the efficacy of N-Acetylcysteine in severe COVID-19 patients: a randomized controlled phase III clinical trial
Bandare-abbas University of Medical Sciences0 sites40 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Bandare-abbas University of Medical Sciences
- Enrollment
- 40
- Status
- Not yet recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All COVID\-19 patients whose disease has been confirmed by the PCR test for SARS\-Cov\-2\.
- •Having one of the criteria for severe COVID\-19 disease includes tachypnea (respiration rate\> 30 per minute), hypoxemia (O2 \= saturation, arterial oxygen partial pressure ratio \<300\), pulmonary infiltration (\> 50% of lung area during 24 48 h), LDH\> 245 U / l, Progressive lymphopenia.
- •Hospitalized in the intensive care unit.
- •Signing the written consent of the study participant.
Exclusion Criteria
- •Known allergy or hypersensitivity to N\-Acetylcysteine.
- •The participant refused to participate in the continuation of the study.
Outcomes
Primary Outcomes
Not specified
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