N/A
N=599
Dialysis Catheter Comparative Clinical Trial
End Stage Renal Disease
Bottom Line
View on ClinicalTrials.gov: NCT00526123 ↗Enrolled (actual)
599
Serious AEs
2.5%
Results posted
Jan 2013
Primary outcome: Primary: First Catheter Induced Complication — 78; 77 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Symmetric Tip Catheter (Device); Conventional Split-tip Catheter (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Tyco Healthcare Group
- Primary completion
- Aug 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY First Catheter Induced Complication |
40; 48 | — |
| PRIMARY First Catheter Induced Complication |
40; 48 | — |
| PRIMARY First Catheter Induced Complication |
40; 48 | — |
| SECONDARY Inadequate Flow Rates Requiring Surgical/Radiological Intervention |
18; 29 | — |
| SECONDARY Average Number of Line Reversals Per Subject |
6.5; 8.0 | — |
| SECONDARY Frequency of Clinician Interventions for Catheter Malfunction and Infection |
8.2; 10.0 | — |
| SECONDARY Primary Failure Rate |
3.9; 4.9 | — |
| SECONDARY Reliability of the Catheter |
90.6; 86.9 | — |
Summary
The purpose of this clinical trial is to compare the longevity of two dialysis catheters.
Eligibility Criteria
Inclusion Criteria
- Subject must be 18 years of age or older.
- Subject must meet labeled indication for hemodialysis.
- Subject must have End Stage Renal Disease (ESRD).
- Subject must have a patent right or left internal jugular vein.
- Subject treatment plan must require chronic hemodialysis treatments 3 times per week for a minimum of 6 weeks.
- Subject must give written informed consent.
Exclusion Criteria
- Subjects who are concurrently enrolled in any Randomized Clinical Trial (RCT) or those that may enroll in a RCT during the course of the study, or subjects who have been previously randomized into this clinical study.
- Subjects with active infection at the time of study enrollment.
- Subjects with a known sensitivity to heparin, or previous incidence of heparin-induced thrombocytopenia.
- Subjects with uncontrolled abnormal coagulation parameters and are at additional risk for clotting or excessive bleeding.
- Subjects who are known or suspected to be pregnant at the time of study enrollment or plan to get pregnant during the study period.
- Subjects for whom performing dialysis at flow rates up to 450 mL/min would be contraindicated for any reason.
- Subject unable or unwilling to commit to follow-up visits and study procedures throughout the course of the study.
- Subjects who, in the opinion of the Investigators, are not appropriate candidates for the study based upon current or past medical history, or negative past experience with either of the study catheters.
Data sourced from ClinicalTrials.gov (NCT00526123). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.