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Comparison of External Jugular Vein to Internal Jugular Vein in Critically Ill Patients.

Comparisons of the Outcomes of Venous Access through External Jugular Vein versus Internal Jugular Vein Using Central Venous Catheter in Patients Admitted to Intensive Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043489
Enrollment
200
Registered
2022-06-24
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: - Health Condition 2: J069- Acute upper respiratory infection,unspecified Health Condition 3: K709- Alcoholic liver disease, unspecified Health Condition 4: O- Medical and Surgical Health Condition 5: G01- Meningitis in bacterial diseases classified elsewhere Health Condition 6: D499- Neoplasm of unspecified behavior of unspecified site Health Condition 7: B998- Other infectious disease Health Condition 8: 8- Other Procedures Health Condition 9: B954- Other streptoco

Interventions

Intervention1: EJV: EJV cannulation using simple cannula for 14 days. Control Intervention1: IJV: IJV cannulation with seven french catheter for 14 days

Sponsors

Department of Critical Care Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex and all age admitted to Intensive care unit. 2. Patients requiring vasopressor. 3. Patients requiring veno-irritant and hyperosmolar drugs. 4. Patients with poor peripheral venous access. 5. Patients requiring long term venous access. 6. Patients following cardiac arrest.

Exclusion criteria

Exclusion criteria: 1. Patients with cervical cord injury 2. Patients with insertion site infection/surgery/injury. 3. Patients requiring haemodialysis 4. Patients requiring TPN

Design outcomes

Primary

MeasureTime frame
ââ?¬Â¢ To assess technical success of procedure ââ?¬Â¢ To assess procedural complication ââ?¬Â¢ To assess delayed complication (CRBSI, catheter malfunction) Timepoint: baseline and 2 weeks.—

Secondary

MeasureTime frame
ââ?¬Â¢ To assess catheter dwell time.Timepoint: Week 1—

Countries

India

Contacts

Public ContactPriyank kumar singh

Bharati Hospital and Research Centre

suchetashiva@gmail.com9822051719

Outcome results

None listed

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