At a glance
ClinicalIndex Comparison RecordN/ACompleted· 378 enrolled
Drug / intervention
Intravenous Access Device Flushingdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Prospective, Multi-center, Randomized, Open Label, Controlled Trial of BD Pre-filled Flush Syringes
In Brief
A clinical study evaluating Intravenous Access Device Flushing for Effectiveness and Safety of Pre-filled Flush Syringe. Completed, enrolled 378 participants across 3 sites.
Detailed Summary
This study is to compare the BD PosiFlush™ Pre-filled Flush Syringes (manufactured by BD, USA) and evaluate the effectiveness and safety of the pre-filled flush syringes (manufactured by Suzhou Becton Dickinson Medical Devices Co., Ltd.) for locking and flushing the end of catheter line in Chinese popluation.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--
Timeline
N/ACompletedFinished
2023202420252026
Enrollment StartNov 2022
First PostedMar 2023
Primary CompletionDec 2023
TodayJul 2026
First PostedMar 10, 2023
Enrollment StartNov 3, 2022
Primary CompletionDec 26, 2023
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 3.3 years ago
Interventions
Intravenous Access Device Flushingdevice
locking and flushing the end of catheter line at the intervals of different drug treatment.