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Treatment of Hemodialysis Catheter-Related Bacteremia

University of California San Diego logo

University of California San Diego

Status and phase

Withdrawn
Phase 3
Phase 2

Conditions

Hemodialysis Catheter-related Bacteremia

Treatments

Device: guide-wire exchange
Drug: tigecycline, N-acetylcysteine, heparin combination

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02040818
RCT 131309

Details and patient eligibility

About

Patients who undergo hemodialysis via a tunneled catheter often develop bloodstream infections that arise from the catheter. There are several management options for treatment of such an infection, though the best option is not clearly delineated. Standard of care options include exchanging the catheter for a new one over a guide-wire and instilling a high concentration of an antibiotic directly into the catheter lumen. The investigators are planning to treat hemodialysis catheter bloodstream infections by one of two strategies: 1. Use of a novel antibiotic lock solution Or 2. Changing out the infected catheter for a new one. Both these options have comparable cure rates as shown in the medical literature. After obtaining informed consent, patients will be randomized to either treatment arm and will continue to receive all other standard medical care.

Specific Aim: To conduct a randomized clinical trial to demonstrate that the use of a novel antibiotic lock solution (consisting of N-acetylcysteine, tigecycline and heparin) is non-inferior to guide-wire exchange in the treatment of hemodialysis catheter-related bacteremia.

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any adult (≥ 18 years of age) who has ESRD and a prevalent or incident tunneled hemodialysis catheter with bacteremia will be eligible for enrollment.

Exclusion criteria

  • The following patients will be excluded: 1) patient is unable (and no guardian or legal representative is available) or unwilling to provide informed consent, 2) patient is allergic to NAC, tigecycline, minocycline, or heparin, 3) patient has evidence of a complicated bacteremia such as endocarditis, septic thrombophlebitis, septic emboli, osteomyelitis, deep seated abscess, or hypotension requiring use of vasopressors, 4) patient has evidence of an exit site infection around the catheter such as a pus pocket, purulent drainage, or erythema, 5) patient is pregnant or will become pregnant, 6) the infection is due to an organism that is resistant to tigecycline such as Candida or Pseudomonas species.

Trial design

0 participants in 2 patient groups

Antibiotic Lock Solution
Experimental group
Treatment:
Drug: tigecycline, N-acetylcysteine, heparin combination
Guide-wire Exchange
Active Comparator group
Treatment:
Device: guide-wire exchange

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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