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Ultrasound guided femoral venous cannulation:A Randomised Controlled trial.

Ultrasound guided oblique view versus transverse view in femoral venous cannulation:A Randomised Controlled trial. - NIL

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/059133
Enrollment
80
Registered
2023-10-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: 2- Placement

Interventions

Intervention1: ultrasound guided oblique view in femoral vein canulation: In oblique view the Probe will be placed in transverse axis view, then slowly rotating to oblique axis view to visualize the m

Sponsors

AIIMS Bhubaneswar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a)Indication for central venous cannulation is there

Exclusion criteria

Exclusion criteria: a) Skin infection and previous history of surgery at the site b) INR >2 and platelet count c) Femur fracture in trauma d) Age 65 yrs e) Pregnancy f) Refusal to participate g) Obesity(BMI >30)

Design outcomes

Primary

MeasureTime frame
Our primary outcome is to assess the performing time (in sec) for cannulating femoral vein in both the views of ultrasound. Performing time is defined as the time duration from puncture of skin to visualization of the guidewire in the femoral vein. Timepoint: 0 ,1, 5,15,30 mins

Secondary

MeasureTime frame
is to record the incidence of arterial puncture, local hematoma, femoral vein thrombosisTimepoint: 0,30 mins, 6hr, 24hr

Countries

India

Contacts

Public ContactDR Surojit Roy

AIIMS BHUBANESWAR, ODISHA

drsangeeta.asth@gmail.com09556547655

Outcome results

None listed

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