Spironolactone in Covid-19 Induced ARDS

NCT04345887 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2021-10-28

No results posted yet for this study

Summary

This study intended to evaluate the effects of commonly used diuretic, spironolactone, on oxygenation in covid-19 ARDS patients.

Conditions

  • Respiratory Distress Syndrome, Adult

Interventions

DRUG

Spironolactone 100mg

2x100 mg spironolactone for 5 consecutive days

DRUG

Placebo oral tablet

2 x1 placebo tablet

Sponsors & Collaborators

  • Istanbul University - Cerrahpasa

    lead OTHER

Principal Investigators

  • Yalim Dikmen · Prof

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-05-05
Primary Completion
2020-06-15
Completion
2020-07-05

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04345887 on ClinicalTrials.gov