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Melatonin in COVID-19

Inflammation control in patients with COVID-19 using melatonin supplement compare to controls referred to Imam Khomani Hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200922048804N1
Enrollment
20
Registered
2020-10-06
Start date
2020-08-05
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

COVID-19. Clinically-epidemiologically diagnosed COVID-19

Interventions

Intervention 1: Intervention group: Prescribing 6 mg of melatonin capsules made by Elite factory for 2 weeks, which should be consumed half an hour before bedtime every night in low light conditions a

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: mild to moderate patients with COVID-19 who receive Hydroxy chloroquine Confirmation of the disease is based on CT scan and clinical symptoms and physician diagnosis Patients 25-65 years

Exclusion criteria

Exclusion criteria: Patient with depression, COPD, sleep apnea and seizure Patients with severe kidney problem (eGFR<30 ml/min) Patients with severe liver problem Patients who receive fluvoxamine, benzodiazepine or zolpidem patients who receive drugs that extends QT Pregnant and breastfeeding mothers Patients who have allergy to melatonin

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: 10-14 days. Method of measurement: COVID-19 questionnaire.;Lung infection. Timepoint: 10-14 days. Method of measurement: CTscan and physician diagnosis.;CRP ( C reactive protein). Timepoint: 10-14 days. Method of measurement: Lab test.;Fever. Timepoint: 10-14days. Method of measurement: questionnaire.;Vomiting. Timepoint: 10-14 days. Method of measurement: Questionnaire.;No smelling. Timepoint: 10-14 days. Method of measurement: questionnaire.;No taste. Timepoint: 10-14 days. Method of measurement: questionnaire.;Cough. Timepoint: 10-14 days. Method of measurement: Questionnaire.;Respiratory distress. Timepoint: 10-14days. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Alizadeh

Immunology, Asthma & Allergy Research Institute

zalizade@yahoo.com+98 21 6693 5855

Outcome results

None listed

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