Using blood tests to predict infections after kidney stone surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to develop a risk stratification system for predicting postoperative infectious complications and systemic inflammatory responses in patients undergoing percutaneous nephrolithotomy (PCNL). By analyzing pre-and post-operative blood endotoxin levels, the researchers hope to identify patients at higher risk for infections. The study will involve adults scheduled for PCNL at Uhealth tower and Jackson Memorial Hospitals, focusing on their blood profiles before and after the procedure.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults that is able to consent (≥ 18 years of age)
* Scheduled to undergo PCNL at Uhealth tower and Jackson Memorial Hospitals
* not currently immunosuppressed \[White blood count (WBC) \>= 2, not on immunosuppressive medications\]

Exclusion Criteria:

* unable to consent and \< 18 years of age
* currently immunosuppressed (WBC \< 2, not on immunosuppressive medications)

Where it's running

• University of Miami
  Miami, Florida, United States Recruiting

Study contacts

• Principal investigator: Hemendra N Shah — University of Miami
• Study coordinator: Hemendra N Shah
• Email: hns35@miami.edu
• Phone: 3052433246

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Early versus delayed shock wave treatment for leftover kidney stones after percutaneous nephrolithotomy

  This trial tests whether doing extracorporeal shock wave lithotripsy (ESWL) early or waiting longer after PCNL helps clear leftover kidney stone fragments ≤15 mm with fewer complications.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.