Device Related Infection

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Review clinical trials related to Device Related Infection. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The IVCare Adaptive Platform Trial

The IVCare trial is a multicentre adaptive platform study evaluating interventions to prevent infections and other complications associated with central venous access devices (CVADs) in patients with newly inserted or existing devices. The study is organised into domains addressing different aspects of CVAD care and includes patient groups referred to as strata. Domains, strata and interventions may change over time as the study progresses. IVCare also includes an observational cohort study in which patients with CVADs are followed to assess CVAD care practices, infections, and other CVAD-related complications across health services. The trial starts with two domains. The Connectors/Caps Domain compares antimicrobial chlorhexidine-containing connectors and caps with standard-of-care connectors and caps used in Australian hospitals. In the cancer stratum, participants are randomised to receive either InVision-Plus CS® or standard-of-care connectors/caps. In the kidney disease stratum, participants are randomised to receive either ClearGuard™ HD or standard-of-care connectors/caps. Following a predefined stopping decision for ClearGuard™ HD in the kidney disease stratum, Tego™ will be introduced and evaluated in this group. The Securement Domain compares the effectiveness of SecurAcath®, a subcutaneous anchor securement system, with standard-of-care securement methods used in Australian hospitals. Participants in both the cancer and kidney disease strata are randomised to receive either SecurAcath® or standard-of-care securement.

Participants needed: 2,500
Trial details
Biological sex: AllType: InterventionalSponsor: The University of QueenslandUpdated: May 14, 2026
Eligibility criteria

The patient has or requires a CVAD, including a PICC, a non-tunnelled or tunnell... [+1]

Central line-associated bloodstream infection (CLABSI) currently suspected assoc... [+15]

Status: Not yet recruiting

Chlorhexidine Caps for CLABSI Prevention in Hemodialysis: a Pilot Randomized Controlled Trial

The goal of this clinical trial is to compare a chlorhexidine antimicrobial barrier cap in patients requiring hemodialysis treatment to the standard hemodialysis caps currently used within the Metro North Kidney Health Service. The main questions to answer are: * Study Feasibility * Occurrence of infectious complications related to renal central venous catheters Participants will be randomly allocated to receive either of the below hemodialysis caps to cover their hemodialysis catheter hub: * The standard hemodialysis cap used at the Royal Brisbane and Women's Hospital, or * The intervention hemodialysis cap containing chlorhexidine inside it Researchers will compare standard and chlorhexidine hemodialysis caps to see if the presence of chlorhexidine improves the occurrance of infectious complications related to the hemodialysis catheter.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of QueenslandUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

Age≥18 [+4]

Current CLABSI [+3]

Status: Not yet recruiting

Application of Radiomics for Diagnosis and Follow-up of Cardiovascular Device Infections: PREDICT Study

Single center, open-label, phase IV clinical trial to study the application of radiomics in molecular imaging for diagnosis and follow-up of CVDIs. The study will include three populations: * Retrospective cohort (2018-2025) * Prospective cohort (2026-2027) * Control group (prospective)

Participants needed: 200
Trial details
Phase: Phase 4Age: 18-84Biological sex: AllType: InterventionalSponsor: Fundacion Clinic per a la Recerca BiomédicaUpdated: Mar 6, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+5]

Inability to undergo FDG-PET due to contraindications (e.g., allergies, claustro... [+3]