The clinical study of a new subclavian venipuncture improved technology

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-TRC-12002765

Enrollment

Unknown

Registered

2012-12-07

Start date

2012-02-29

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

subclavian venipuncture

Interventions

Two groups:Modified subclavian puncture versus Traditional subclavian puncture

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. patients admitted to the principle of voluntary and signed informed consents; 2. the need to line deep vein catheterization patients; 3. the age of 18-65 years of age, male or female; 4. no significant shock performance; 5. with severe heart, lung, nervous system disease.

Exclusion criteria

Exclusion criteria: 1. does not agree to participate in a study of patients in this trial; 2. age 65 years; 3. with severe heart and lung disease; 4. local history of trauma, and other anatomical deformity; 5. the local 3 times more Cannulax history; 6. severe obesity, body mass index, BMI> 30.

Design outcomes

Primary

Measure	Time frame
Puncture success rate;	—

Countries

China

Contacts

Public ContactFu Guo-qiang

Fuguoqiang201010@hotmail.com+86 021 20256301

Outcome results

None listed

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