Clinical Trials Directory

Trials / Completed

CompletedNCT02189434

Does Serum Procalcitonin Levels Predict Sepsis in Patients Undergoing Cytoreductive Surgery

A Pilot Study to Determine the Correlation of Serum Procalcitonin Levels and Development of Sepsis in Patients Undergoing Cytoreductive Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
Eastern Regional Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Serum procalcitonin levels will be considerably higher, for a longer period of time, in patients who develop sepsis compared to patients with SIRS or those who have an uncomplicated post-surgical recovery. Monitoring of serum procalcitonin trends will allow for an earlier diagnosis of, and initiation of treatment for, sepsis compared to current standard ICU methods.

Conditions

Interventions

TypeNameDescription
OTHERSerum procalcitonin lab drawsBlood will be collected in a 4mL capacity, green top lithium heparin tube. Samples can be drawn from a port with other labs. The samples will be centrifuged and then the plasma/serum will be removed and placed into a screw-capped round bottom plastic vial. Samples will be stored at -20○C until processing. Serum samples will be batch processed for each participant at the conclusion of their study period. These draws will be conducted for the sole purpose of this study, and whenever possible, they will be performed at the same time as routine blood draws conducted for medical monitoring to reduce the burden to the patients.

Timeline

Start date
2014-06-01
Primary completion
2016-04-01
Completion
2016-04-01
First posted
2014-07-14
Last updated
2017-07-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02189434. Inclusion in this directory is not an endorsement.