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Study identifier: NCT06002607 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Shorter Versus Extended Course of Antibiotic Therapy for Necrotizing Soft Tissue Infections

Condition: Necrotizing Soft Tissue Infection  ·  Sponsor: University of California, Irvine

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Necrotizing soft tissue infection (NSTI) is a devastating disease that results in a high rate of in-hospital complications and despite advances in critical care, wound care, and early intervention, NSTI continues to be associated with a mortality rate of nearly 30%. The antibiotics used in this treatment are Clindamycin, Vancomycin, Piperacillin Tazobactam; these antibiotics may be administered combined or individually, based on individualized patient treatment. Although one of the tenets of management for NSTI is early broad-spectrum intravenous antibiotics (listed above), the duration of antibiotics needed is not well defined. Currently, there exists wide variation in the duration of antibiotics for NSTI ranging between 2-16 days. The objective of this study is to evaluate the safety of a shorter course of antibiotics hypothesizing that a short duration of antibiotics for 48-hours after source-control is achieved will have similar risk of morbidity and mortality compared to a 7-day course of antibiotics post source control. A second aim of this study will be to identify if serum procalcitonin levels/ratio correspond to resolution of systemic infection in patients with NSTI.

This description comes directly from the study's public registry record.

Talk to the study team

Areg Grigorian, MD  ·  8184389093  ·  agrigori@hs.uci.edu

Jeffry Nahmias, MD  ·  9493073035  ·  jnahmias@hs.uci.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of California Irvine Medical CenterOrange, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06002607