Observational Study of Complications Related to Use of Peripherally Inserted Central Catheters (NCT01578993) | Clinical Trial Compass
CompletedNot Applicable
Observational Study of Complications Related to Use of Peripherally Inserted Central Catheters
United States101 participantsStarted 2012-08
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
What they're measuring
1
Rate of PICC Line Occlusions
Timeframe: Insertion to Removal / maximum 3 months