HAT for the Treatment of Sepsis Associated With NASTI

  • STATUS
    Recruiting
  • participants needed
    132
  • sponsor
    Ascension Via Christi Hospitals Wichita, Inc.
Updated on 3 December 2022
thiamine

Summary

Evaluate the impact of HAT therapy versus placebo in the treatment of patients with an acute NSTI and sepsis.

Description

Primary outcome:

  1. Hospital survival

Secondary outcomes:

  1. Duration of vasopressor therapy
  2. Requirement for renal replacement therapy in patients with Acute Kidney Injury (AKI)
  3. ICU length of stay (LOS)
  4. Change in serum procalcitonin (PCT) over first 72 hours
  5. Change in SOFA score over first 72 hours (measured as SOFA score daily for four days, with day one being admission, then 3 days after, totaling 4 days of treatment with HAT)
  6. Procalcitonin clearance (formula = initial PCT - 72 hour PCT divided by initial PCT x 100)
  7. Number of wound related surgeries
  8. Wound status at time of hospital discharge:
  9. Open
  10. Closed

Details
Condition Necrotizing Soft Tissue Infection, Sepsis
Treatment Placebo, HAT, HAT
Clinical Study IdentifierNCT05157360
SponsorAscension Via Christi Hospitals Wichita, Inc.
Last Modified on3 December 2022

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