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A randomized controlled trial on routine replacement of intravenous catheter and clinical symptoms

A randomized controlled trial on routine replacement of intravenous catheter and clinical symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17010879
Enrollment
Unknown
Registered
2017-03-15
Start date
2017-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

nursing

Interventions

Invervention Grope:Daily researchers will evaluate and register the catheter, including blood vessels, medication, the patients' demands. Extubation of the patient will be recorded the causes of extub
Control:Traditional method

Sponsors

Department of Hematology, Xinqiao Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. 18 years of age or older; 2. The consent was obtained from the patients themselves or their guardians; 3. The expected duration of treatment by pivc was greater than 4 days.

Exclusion criteria

Exclusion criteria: 1. Bloodstream infected currently; 2. Planned removal of venous catheter in 24 hours; 3. Venous catheter has been retained for more than 72 hours; 4. Immunocompromised patients or immunosuppressive curers.

Design outcomes

Primary

MeasureTime frame
Retaining time;Phlebitis;—

Countries

China

Contacts

Public ContactDahua Lan

Department of Hematology, Xinqiao Hospital, Third Military Medical University

10662692@qq.com+86 13628450512

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026