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Effect Of Calcitriol On Neutrophil To Lymphocytes Ratio And High Sensitivity C-Reactive Protein Covid-19 Patients

U

Universitas Sebelas Maret

Status and phase

Completed
Phase 2

Conditions

COVID-19

Treatments

Other: Placebo
Drug: Calcitriol

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full 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.

Enrollment

16 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • COVID-19 patients, hospitalized patients, and patients aged 18-60 years

Exclusion criteria

  • pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

16 participants in 2 patient groups, including a placebo group

Control
Placebo Comparator group
Description:
Placebo 2x1 per day
Treatment:
Other: Placebo
Calcitriol
Experimental group
Description:
the treatment group received calcitriol 2x400 iu per day for 5 day
Treatment:
Drug: Calcitriol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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