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Comparative Evaluation of Ultrasound Guided Supraclavicular and Infraclavicular Subclavian Venous Catheterizations in Adult Patients Undergoing Major Surgeries

P

Post Graduate Institute of Medical Education and Research, Chandigarh

Status and phase

Completed
Phase 4

Conditions

Compare Central Line Insertion of Subclavian Vein With Two Different Approaches Using Ultrasound

Treatments

Procedure: ultrasound guided central venous cannulation

Study type

Interventional

Funder types

Other

Identifiers

NCT02925715
INT/IEC/2015/321

Details and patient eligibility

About

Comparison of two techniques of central venous cannulation of subclavian vein using ultrasound was performed. ultrasound guided central venous cannulation is the standard practice today but its use in subclavian vein is technically challenging and not much literature is available. In this study 96 Patients were randomized into one of the groups and compared for various outcomes. The primary outcome studied was the time taken for procedure. Secondary objectives included comparison of total access time using both the techniques,comparison of first attempt success rate, comparison of the quality of needle visualization and the comparison of immediate (mechanical) and delayed complication rates.

Enrollment

96 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults requiring central venous cannulation.

Exclusion criteria

  • History of prior catheterization.
  • Limited sites for access attempts (other catheters, pacemaker, prior surgery).
  • Previous difficulties during catheterization such as more than three punctures at one site, two sites attempted or failure to gain access.
  • Previous mechanical complications during catheterization.
  • Patients with infection at puncture site and contralateral pneumothorax.
  • Patients with trauma to clavicle and upper ribs, distorted anatomy of neck or clavicles.
  • Cervical spine injury.
  • Known vascular abnormality.
  • Untreated coagulopathy such as International Normalization Ratio(INR) ≥ 2, activated partial thromboplastin time >1.5 of normal or platelets <50,000/mm3
  • After 3 attempts at needle puncture.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

96 participants in 2 patient groups

supraclavicular
Experimental group
Description:
ultrasound guided central venous cannulation done by supraclavicular approach
Treatment:
Procedure: ultrasound guided central venous cannulation
infraclavicular
Experimental group
Description:
ultrasound guided central venous cannulation done by infraclavicular approach
Treatment:
Procedure: ultrasound guided central venous cannulation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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