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Evaluating the effect of Marshmallow and Licorice on COVID 19 patients

Phase 3
Recruiting
Conditions
COVID 19.
Corona virus infection, unspecified
U07.1
Registration Number
IRCT20200404046937N1
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Age =18 years
Laboratory polymerase chain reaction (PCR) confirmed infection with COVID19.
Lung involvement confirmed with chest imaging
Hospitalized with: Fever (axillar or oral temperature = 38.0 °centigrade(C) or =38.6°centigrade tympanic or rectal) or Respiratory rate >24/min Or Cough
Less than 8 days since illness onset
Willingness of study participant to accept randomization to any assigned treatment arm.
Acceptance of non-participation in another study before the 28th day of the study

Exclusion Criteria

Physician makes a decision that trial involvement is not in patients' best interest, or any condition that does not allow the protocol to be followed safely.
Severe liver disease
Oxygen saturation=94%
Known allergic reaction to Marshmallow or Licorice
Severe renal impairment
Pregnant or breastfeeding women
Transfer to another non-study hospital within the next 72 hours
Receipt of any experimental treatment for COVID 19 within the 30 days prior to the time of the screening evaluation.
Angiotensin converting enzyme (ACE) inhibitor users
Hypertensive patients

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Viral diagnostic test. Timepoint: The first day of the study and the end of the study (10th day). Method of measurement: Polymerase chain reaction.
Secondary Outcome Measures
NameTimeMethod
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