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Is it feasible for chindren patients to draw blood sample from peripheral venous catheter?- A randomized controlled trial

Is it feasible for chindren patients to draw blood sample from peripheral venous catheter?- A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOR-17012962
Enrollment
Unknown
Registered
2017-10-12
Start date
2017-10-09
Completion date
Unknown
Last updated
2017-10-16

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

Conditions

The chindren patients who need both peripheral venous catheter and blood collection

Interventions

Control Group:Routine blood collection
Trial group:Peripheral venous catheter combined with vacuum tube for blood collection

Sponsors

The First Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: 1. Patients need to draw blood collection; 2. patients need to puncture peripheral venous catheter; 3. Both male and female between 0-14 years of ages; 4. Patients voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with hemolytic disease, such as hemolytic disease of newborn, burns. 2. Abnormal coagulation function or undergoing thrombolysis or anticoagulant therapy(e.g. DIC); 3. Patients with poor compliance; 4. Other cases which researchers believe that can not enroll.

Design outcomes

Primary

MeasureTime frame
Rate of hemolysis;

Secondary

MeasureTime frame
The qualified rate of the sample;The success rate for the first puncture;The occurrence and time of complications;Patients satisfaction;Time-consuming of sample collection;

Countries

China

Contacts

Public ContactDongqin Shen

The First Hospital of Lanzhou University

shendq2001@163.com+86 09318356292

Outcome results

None listed

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