Serum Endotoxin Assay to Predict the Development of Postoperative Infectious Complications and Systemic Inflammatory Response Following Percutaneous Nephrolithotomy.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Miami

About this trial

The aim of the study is to establish an infectious risk stratification system based on pre-and post-operative blood endotoxin profile.

Eligibility criteria

Qualifiers

Adults that is able to consent (≥ 18 years of age)

Scheduled to undergo PCNL at Uhealth tower and Jackson Memorial Hospitals

not currently immunosuppressed [White blood count (WBC) >= 2, not on immunosuppressive medications]

Disqualifiers

unable to consent and < 18 years of age

currently immunosuppressed (WBC < 2, not on immunosuppressive medications)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

150 Participants
are grouped into 1 trial group

Sponsors and collaborators