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Survey of Practices Regarding the Use of Taurolidine Lock Solutions in Patients With Insertion of a Peripherally Inserted Central Catheter (PICC) in a Vascular Access Unit (TAURO-USE2)

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Not yet enrolling

Conditions

Taurolidine Lock Solution

Study type

Observational

Funder types

Other

Identifiers

NCT07259421
38RC25.0315.

Details and patient eligibility

About

The primary objective of this study is to describe current practices regarding the administration of taurolidine lock solutions in relation to medical prescriptions for patients who have undergone peripherally inserted central catheter (PICC) implantation in the Vascular Access Unit as part of parenteral nutrition therapy. Our underlying hypothesis is that the use of taurolidine lock solutions may deviate from current recommendations, particularly with respect to administration procedures.

This study will allow us to characterize the use of taurolidine lock solutions in relation to medical prescriptions, identify potential deviations from recommended practices, and document any associated adverse events. It will also enable follow-up of PICC outcomes at 8 and 30 days after implantation in the Vascular Access Unit, whereas current follow-up is performed only at 8 days post-insertion.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient who has undergone PICC placement in the vascular access unit with an indication for parenteral nutrition supplementation.
  • Patient not opposed to participating in this research.

Exclusion criteria

  • Patient not speaking French
  • Patient under guardianship or conservatorship
  • Patient with major neurocognitive disorders
  • Patient with severe hearing impairment
  • Patient who do not have a telephone

Trial contacts and locations

0

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Central trial contact

Cordélia SALOMEZ-IHL, pharmacist; Aida MANDZO, clinical research associate

Data sourced from clinicaltrials.gov

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