A comparative study of two types of central venous cannulations, subclavian vein and brachiocephalic vein in adult neurosurgical patients

Completed

• Conditions: Other Procedures,

• Registration Number: CTRI/2023/09/058169
• Lead Sponsor: Shijas m

Brief Summary

After obtaining Institutional Research Committee and Ethical Committee approval, 84 patients will be selected based on inclusion and exclusion criteria. Informed written consent shall be obtained from the patient and a primary care giver of the patient.Eighty four patients who are willing to be a part of the study will be allocated to two groups of 42 patients each- Group SCV and Group BCV using convenient sampling.Procedure will be performed by a consultant anaesthesiologist having a 5 year of experience  after induction and intubation. A portable Mindray USG scanner (2D) mode with a linear transducer probe of 5-12 MHz will be used. Under aseptic precautions, preparation and draping of the cannulation site will be done.Under usg guidence right infraclaviculae subclavian vein and supraclavicular brachiocephalic vein will be cannulated.

Now the trial is ongoing. We started recruiting the subjects to both the groups based on the inclusion and exclusion criterias.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-01-10
• Study Completion: 2024-11-21
• Last Update Posted: 2025-03-30

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 84

Inclusion Criteria

1.Patients posted for elective neurosurgical procedures,requiring central venous cannulation 2.Patients with American society of anasethesiologists physical status I and II 3.Height between 150-170 cm.

Exclusion Criteria

1.Patient refusal 2.Coagulopathy 3.Infection at cannulation site 4.Patients with central venous catheter insitu/history of right sided central venous catheter in the past 5.Patients with vervical trauma with neck immobilisation.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
First attempt success rate	1.5 Years
Overall success rate	1.5 Years

Secondary Outcome Measures

Name	Time	Method
1.Overall success rate	2.Procedural ease

Trial Locations

Locations (1)

Government medical college hospital kozhikode; 🇮🇳 Kozhikode, KERALA, India

Government medical college hospital kozhikode

🇮🇳Kozhikode, KERALA, India

Dr Shijas m

Principal investigator

9562972414

shijas5630@gmail.com