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NCT03711227

Procalcitonin at Zero and 24 Hours as a Prognostic Factor in Patients With Pneumonia

Completed Last updated 29 November 2024
What this trial tests

trial testing Procalcitonin lab test in Pneumonia in 185 participants. Completed in 1 August 2019.

Timeline
17 July 2018
Primary endpoint
1 August 2019
1 August 2019

Quick facts

Lead sponsorCorewell Health South
StatusCompleted
Study typeOBSERVATIONAL
Enrollment185
Start date17 July 2018
Primary completion1 August 2019
Estimated completion1 August 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Corewell Health South — full company profile →

Who can join

18 and older, any sex, with Pneumonia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Procalcitonin levels checked initially and at 24 hours will correlate with disease severity, morbidity, and mortality. Patients who have a higher procalcitonin level initially and at 24 hours will likely have higher qSOFA scores, longer lengths of stay, longer duration of antibiotics and higher 30 day mortality rates.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Pneumonia

Currently open trials in the same condition.

Other Corewell Health South trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03711227.

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