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Effectiveness of HMD 99 capsule (St. John’s wort and Lemon Balm extract along with DDW water) in the treatment of patients with COVID-19 disease

Effectiveness of HMD 99 capsule (St. John’s wort and Lemon Balm extract along with DDW water) in the treatment of patients with COVID-19 disease referred to Imam Khomeini Hospital in Tehran: a randomized double blind clinical trial study.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210216050373N2
Enrollment
110
Registered
2021-12-19
Start date
2022-01-04
Completion date
Unknown
Last updated
2022-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid-19. COVID 19, virus identified

Interventions

Sponsors

Imam Khomeini Hospital, Tehran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: To participate in the study, patients, or their legal guardian must give their knowing and voluntary consent in writing and orally The PCR test for SARS-CoV-2 virus must be positive with one of the following conditions: signs indicating covid-19 disease such as fever, dry cough and shortness of breath CT scan (HRCT or Spiral CT) to show coronavirus involvement, specifically in the ground glass view in the peripheral or basal portions of the lungs and physician's confirmation Patients who have signs of medical conditions secondary to covid-19 infection such as Acute Respiratory Distress Syndrome (ARDS) or myocarditis Patients should not have taken antiretroviral or boosters of immune system up to 3 months prior to the start of the study

Exclusion criteria

Exclusion criteria: Patients will not participate in this study during pregnancy or lactation Patients whose covid-19 infection has not been confirmed but have cold or flu-like symptoms. Current use of stimulants or depressant drugs or alcohol Use of growth hormone, testosterone or anabolic steroids up to 30 days prior to the start of the study Long-term treatment with immunosuppressant medications except topical steroids Patients undergoing chemotherapy, radiotherapy (up to 3 weeks prior to the start of the experiment) or patients who have been prescribed interferon

Design outcomes

Primary

MeasureTime frame
Blood test (CBC, Diff-ESR-CRP-Ast-Alt-Cr-D Dimer). Timepoint: At the beginning, and after 14 days at the end of the study. Method of measurement: Blood Test CBC, (Diff-ESR-CRP-Ast-Alt-Cr-D Dimer).

Secondary

MeasureTime frame
Clinical manifestations: Respiratory symptoms or common acute and non-respiratory symptoms such as lethargy, fever, myalgia, dry cough, phlegm, diarrhea, shortness of breath, rhinitis, vomiting, headaches, chills. Timepoint: daily for 14 days. Method of measurement: Physician's examination, patients answers, information recorded in patient files.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Ahmad Alinaghi, M.D.

Imam Khomeini Hospital, Tehran

a_alinaghi@sina.tums.ac.ir+98 21 6658 1583

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026