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A Prospective Randomized Controlled Trial on the Success Rate and Safety of Puncture in Different Directions Using Landmark-Guided Femoral Vein Puncture

A Prospective Randomized Controlled Trial on the Success Rate and Safety of Puncture in Different Directions Using Landmark-Guided Femoral Vein Puncture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096775
Enrollment
Unknown
Registered
2025-02-06
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

the Femoral Vein Puncture

Interventions

Experimental group (the lateral approach group):Femoral vein puncture: Lateral approach needle insertion
Control group (the orthogonal approach group):Femoral vein puncture: Orthogonal approach needle insertion

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients in need of femoral vein catheterization; 2. Patients aged >=18 years, <=80 years; 3. ASA physical status: I-IV; 4. BMI<= 25 kg/m^2.

Exclusion criteria

Exclusion criteria: 1. Patients with thrombosis or inflammation in the target vessel 2. Patients with infection at the puncture site 3. Patients who had previously undergone surgery on the femoral vessels or pelvis 4. Patients who had Inguinal hernia or peripheral vascular disease

Design outcomes

Primary

MeasureTime frame
success rate of femoral vein puncture;

Secondary

MeasureTime frame
puncture time;complications;

Countries

China

Contacts

Public ContactTang Bing

Shanghai East Hospital

tbhuya@163.com+86 159 2132 0718

Outcome results

None listed

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