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NCT05402995

Randomized Trial Comparing Irrisept to Saline Irrigation for Infection Prevention

Terminated Phase 4 Results posted Last updated 24 April 2024
What this trial tests

Phase 4 trial testing Irrisept (Irrigation Solution) in Gustilo-Anderson Type III Open Tibia Fracture in 6 participants. Terminated before completion.

Timeline
21 June 2022
Primary endpoint
31 August 2023
31 August 2023

Quick facts

Lead sponsorBrett D. Crist
PhasePhase 4
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment6
Start date21 June 2022
Primary completion31 August 2023
Estimated completion31 August 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Brett D. Crist — full company profile →

Who can join

18 and older, any sex, with Gustilo-Anderson Type III Open Tibia Fracture. Patients with the condition only — healthy volunteers not accepted.

Results — posted to ClinicalTrials.gov

Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.

Number of Participants Experiencing Surgical Site Infection (SSI) Primary · 90 days

Measured by the number of surgical site infections in the total population of patients.

GroupValue95% CI
Standard Operative Debridement and Spanning External Fixator (Reference/Control Group)0
Spanning External Fixator With Irrisept Irrigation (Treatment Group 1)0
Antibiotic-coated Medullary Nail With Saline Irrigation (Treatment Group 2)0
Antibiotic-coated Medullary Nail With Irrisept Irrigation (Treatment Group 3)0

Adverse events — posted to ClinicalTrials.gov

Time frame: 1 year. Reporting threshold: 0%. Adverse-event reports describe events observed during the trial — not all are caused by the drug.

Standard Operative Debridement and Spanning External Fixator (Reference/Control Group)
Serious: 0
Deaths: 0
Spanning External Fixator With Irrisept Irrigation (Treatment Group 1)
Serious: 0/2 (0%)
Deaths: 0/2
Antibiotic-coated Medullary Nail With Saline Irrigation (Treatment Group 2)
Serious: 1/2 (50%)
Deaths: 0/2
Antibiotic-coated Medullary Nail With Irrisept Irrigation (Treatment Group 3)
Serious: 0/2 (0%)
Deaths: 0/2

Serious adverse events (1 terms)

ReactionSystemStandard Operative Debride…Spanning External Fixator …Antibiotic-coated Medullar…Antibiotic-coated Medullar…
AmputationMusculoskeletal and connective tissue disorders

Most-reported serious reactions: Amputation.

Data from ClinicalTrials.gov NCT05402995 adverse events section.

Sponsor's own description

Early debridement and definitive fixation, at the initial operative setting, historically led to no difference in the infection rates for Gustilo-Anderson type III open tibia fractures. However, Lenarz et al. reported that delaying definitive fixation in open tibia fractures could decrease the deep infection rate. At the University of Missouri, the investigators found that staged procedures, including initial debridement-temporary fixation and delayed definitive fixation, did not statistically decrease the rate of deep infection in Gustilo-Anderson type III fractures, prompting the study that is being proposed here. Antibiotic cement coated intramedullary nails have been used in management of infected long bone fractures. Since external fixation and staged debridement did not decrease type III open tibia infection rate, the investigators wanted to consider using antibiotic cement coated nails to deliver antibiotics locally in the acute open fracture setting to prophylactically decrease associated infection rate. Additionally, Irrisept is a wound irrigant that has been used to lower infection rates in different wound settings. To the investigators' knowledge, there are no robust data showing its effectiveness at lowering infection rates in open tibia fracture management. The purpose of this study is to determine the effects of Irrisept and antibiotic nails on lowering deep infection rates in type III open tibia fractures.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing