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Feasibility of Extending the Time for Flushing, Occlusion, and Replacement of Intravenous Infusion Adaptors for Tumor Patients with PICC Catheters During Discharge:A Multicenter, Randomized Controlled, Non-Inferiority Study

Feasibility of Extending the Time for Flushing, Occlusion, and Replacement of Intravenous Infusion Adaptors for Tumor Patients with PICC Catheters During Discharge:A Multicenter, Randomized Controlled, Non-Inferiority Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117884
Enrollment
Unknown
Registered
2026-01-29
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Interventions

Control group:Both groups of patients used Bard Medical Technology Co., Ltd. model 7655405 three-way valve PICC catheters, Beijing Gishield Medical Devices Co., Ltd. model 01C-NC100 infusion connector
Intervention group:Patients in both groups used three-way valve PICC catheters (model 7655405, Bard Medical Technology Co., Ltd.), infusion connectors (model 01C-NC100, Beijing Gishield Medical Device

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 69 Years

Inclusion criteria

Inclusion criteria: (1) Patients with malignant tumors admitted to the research hospital of this project must have a three-way valve PICC initially inserted for chemotherapy, and during the 3-week treatment interval after discharge with the catheter, they must consistently attend the intravenous catheter care clinic of the trial group for catheter maintenance. (2) During the first maintenance visit to the IV therapy clinic of this center after discharge, the catheter function is assessed to be fully patent, with no complications such as infection or symptomatic thrombosis. (3) Patients assessed using the Venous Thromboembolism (VTE) Risk Assessment Scale and the Catheter Thrombosis Risk Assessment Scale are not classified as high-risk. (4) Normal coagulation function, no history of vascular disease, and no contraindications to medication use. (5) Aged 18–69 years, regardless of gender. (6) Patients have unrestricted mobility. (7) Expected survival time >1 month. (8) Patients are willing to participate, cooperate in completing this clinical study, and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) The PICC catheter tip is not located in the middle to lower third of the superior vena cava. (2) Presence of bleeding or coagulation abnormalities, or recent receipt of other anticoagulation therapy. (3) The current treatment interval after the first assessment is less than 3 weeks.

Design outcomes

Primary

MeasureTime frame
Incidence of catheter occlusion;

Secondary

MeasureTime frame
Incidence of catheter-associated infection;Catheter-related symptomatic thrombosis rate;Patient direct costs associated with catheter care/maintenance;Time cost of infusion therapy clinic specialist nurses;

Countries

China

Contacts

Public ContactJiasi Zhang

The First Affiliated Hospital of Army Medical University

13637771933@163.com+86 180 0233 2823

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026