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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05765617
Other study ID # NAP03
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date July 1, 2021
Est. completion date September 30, 2021

Study information

Verified date March 2023
Source Universitas Sebelas Maret
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research is a study that compares the administration of calcitriol with the outcomes of COVID-19 patients


Description:

This research was an observational analytic cohort retrospective study in which the subjects were moderate degree COVID-19 inpatients in Sebelas Maret University Hospital divided into two groups. The control group received standard therapy, while the treatment group received calcitriol 2x400 iu per day.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date September 30, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - COVID-19 patients, hospitalized patients, and patients aged 18-60 years Exclusion Criteria: - pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Calcitriol
The treatment group received calcitriol 2x400 iu per day for five days. Calcitriol uses Oscal, obtained from Kalbe Pharma
Other:
Placebo
Placebo give 2x1 per day for five day

Locations

Country Name City State
Indonesia Universitas Sebelas Maret Hospital Sukoharjo Central Java

Sponsors (1)

Lead Sponsor Collaborator
Universitas Sebelas Maret

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary HsCRP High-sensitivity C-reactive protein (hsCRP) is a marker of inflammation Hs CRP (high sensitive c reactive protein) examination was carried out on the first day of hospitalization and the 5th day of hospitalization
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