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Demonstration project for the application of disposable anti needle infusion devices with needles/infusion needles

Demonstration project for the application of disposable anti needle infusion devices with needles/infusion needles

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104987
Enrollment
Unknown
Registered
2025-06-26
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

None

Interventions

Intervention group:Provide patients with disposable anti needle infusion devices with needles/infusion needles
Control group:Ordinary infusion set with needle/infusion needle

Sponsors

The People's Liberation Army Army Characteristic Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The research nurse has obtained the professional qualification of nurse, with working time of >=1 year, solid basic skills, skilled operation, stable psychological quality, and can objectively fill in the questionnaire; 2. The number of intravenous infusions in the study participant in the month prior to enrollment is no more than 3 times; 3. Study participants voluntarily participate in the trial and sign the informed consent form, be able to communicate well with the investigator and comply with the relevant requirements of the study; 4. Study participants> 18 years old.

Exclusion criteria

Exclusion criteria: 1. Suffering from congenital malformations or developmental disorders, genetic defects, severe malnutrition, etc.; 2. Neurological disease or family history (convulsions, epilepsy, encephalopathy, etc.); History or family history of psychiatric illness; 3. As assessed by the investigator, the person being infused has any disease or condition that may put the subject at unacceptable risk; The infusion patient is unable to meet the requirements of the protocol; Conditions that interfere with the assessment of the response to the infusion needle.

Design outcomes

Primary

MeasureTime frame
Acupuncture injury rate;

Secondary

MeasureTime frame
Patient's pain level;Nurse satisfaction;Success rate of one-time puncture;Rebound failure rate (experimental group only);Incidence of exhaust obstruction;Adverse event incidence rate;Nurse's single operation time;

Countries

China

Contacts

Public ContactXu Yuanchun

The People's Liberation Army Army Characteristic Medical Center (Daping Hospital)

1085631898@qq.com+86 139 8383 1041

Outcome results

None listed

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