Observational Study of Complications Related to Use of Peripherally Inserted Central Catheters (PRISM-1)

Teleflex

Status: Completed

Conditions: Adult Patients With Peripherally Inserted Central Catheters

Study type: Observational

Funder types: Industry

Identifiers

NCT01578993

S-PICC 2012-01

Details and patient eligibility

About

The purpose of this study is to determine the rate and timing of interventions and complications related to the use of peripherally inserted central venous catheters in adult patients.

Enrollment: 101 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or Female Age > 18 years requiring central venous access
• Ability to comply with study requirements
• Written Informed Consent

Exclusion criteria

• Previous enrollment in study
• Current or recent upper extremity thrombosis, occlusion or stenosis
• Previous axillary lymph node dissection
• Skin inflammatory condition or rashes within 15 cm from insertion site
• Pre-existing history of hypercoagulability unrelated to malignant disease
• Participating in trial involving antithrombotic, anticoagulant or anti- infective drug therapies
• Positive blood culture within 48 hours from planned PICC placement
• Known, renal insufficiency with chronic creatinine levels > 1.7 mg/dl