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Thalidomide effects in COVID-19

Phase 3
Recruiting
Conditions
Covid 19.
Covid 19
Registration Number
IRCT20110423006257N3
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
66
Inclusion Criteria

Duration of the symptoms less than 10 days
Lymphocyte count less than 1000 per microliter
Quantitative CRP more than 1.5 times normal
Positive pcr test of covid 19
O2 sat less than 93%
Respiratory rate less than 24
Chest CT scan findings compatible with COVID-19 Pneumonia

Exclusion Criteria

History of chronic disease
Pregnant women, lactating women , sexually active premenopausal women
Loss of consciousness
Liver enzymes more than 5 times normal

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Radiological changes of the lung. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Pulmonary computed topography scan.;Death rate. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: observation.;Length of hospitalization. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: observation.;Blood oxygen saturation. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Pulseoxymeter.
Secondary Outcome Measures
NameTimeMethod
Complete blood count. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Paraclinical.;Erythrocyte sedimentation rate. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Paraclinical.;Interleukin 6. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Paraclinical.;Creatine phosphokinase. Timepoint: Before the intervention and two weeks after the intervention. Method of measurement: Paraclinical.
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