Skip to content

Clinical trial on the incidence of complications related to the insertion of more than one Central Venous Access into the internal jugular vein

Incidence of complications related to multiple Central Venous Access in the internal jugular vein: multicenter randomized non-inferiority clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7nrvmmm
Enrollment
Unknown
Registered
2024-06-06
Start date
2024-07-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Mechanical complication of vascular dialysis catheter

Interventions

The study will be designed as a prospective, randomized, non-inferiority, open, parallel clinical trial with two groups for patient allocation. The patients who, according to preoperative anesthetic p

Sponsors

Hospital Nossa Senhora da Conceição - Grupo Hospitalar Conceição
Lead Sponsor
Santa Casa de Misericórdia de Porto Alegre
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over 18 years of age; ASA I to IV; scheduled for heart surgery; vascular surgeries; abdominal surgeries; major thoracic surgeries; liver transplants; lung transplants; with anesthetic planning for the insertion of at least two central venous catheters

Exclusion criteria

Exclusion criteria: Patients with a previous history of central venous thrombosis; or central venous stenosis; patients under 18 years of age

Design outcomes

Primary

MeasureTime frame
The main outcome considered for calculating the sample size was the incidence of mechanical complications intraoperatively and in the first 24 hours postoperatively. This is of a composite outcome that includes cardiac dysrhythmias, arterial puncture, hematoma, pneumothorax, catheter insertion failure, or inadequate catheter positioning.

Secondary

MeasureTime frame
Mortality within 30 days.;Catheter-related infection.;Length of stay in the ICU. ;Length of hospital stay. ;Central venous catheter malfunction. ;Central venous catheter insertion time. ;Number of attempts to pass each catheter.

Countries

Brazil

Contacts

Public ContactArthur de Almeida

Hospital de Clinicas de Porto Alegre

arthur-ea@hotmail.com+55(048)996675066

Outcome results

None listed

Source: REBEC (via WHO ICTRP)