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Comparison of three methods of treatment in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) with and without coronavirus positive test

Comparison of three methods of treatment in patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) with and without coronavirus positive test (Kovid-19)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140305016852N4
Enrollment
30
Registered
2020-05-04
Start date
2020-04-20
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Coronavirus disease (covid-19). Other coronavirus as the cause of diseases classified elsewhere

Interventions

Intervention 1: Intervention group: In this group, untreated COVID-19 patients are treated with routine treatments and 50,000 units of vitamin D daily for one week. Intervention 2: Intervention group:

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: The patient was admitted to the acute respiratory center Consent to participate in the study Age 15 to above Do not take vitamin C and D supplements No gout Lack of kidney and liver disease No pregnancy or lactation No treatment with anti convulsants

Exclusion criteria

Exclusion criteria: The patient has lung cancer Patients undergoing chemotherapy and radiotherapy If the patient dies If the patient has a decreased level of consciousness If the patient does not want to continue working on the plan

Design outcomes

Primary

MeasureTime frame
Complete recovery of clinical symptoms of 2019 disease. Timepoint: About a week after starting treatment. Method of measurement: Clinical and laboratory questionnaire.;Normalization of chest symptoms in CT scan. Timepoint: About 7 to 14 days after starting treatment. Method of measurement: CT scan result.

Secondary

MeasureTime frame
Improving and normalizing the level of laboratory symptoms. Timepoint: At least 1 to 2 weeks after starting treatment. Method of measurement: Laboratory techniques.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEbrahim Shirzade

Sabzevar University of Medical Sciences

dreshirzad@yahoo.com+98 51 4401 1300

Outcome results

None listed

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