Clinical trial · Interventional
Oblique Versus Transverse Orientation Approach for Internal Jugular Venous Cannulation in Pediatrics
Oblique Versus Transverse Transducer Orientation Approach for Ultrasound Guided Internal Jugular Venous Cannulation in Heart Surgery Pediatric Patients
NCT05656937CI-TRIAL-00062762completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
this study aimed to compare oblique versus transverse orientation approach in jugular venous cannulation in term of cannulation success in pediatric heart surgery patients
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Heart; Surgery, Heart, Functional Disturbance as Result | — | UNRESOLVED | — |
| Pediatric ALL | Childhood Acute Lymphoblastic Leukemia | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| internal jugular venous cannulation | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Oblique orientation
- description
- cannulation will be oblique approach
- interventionNames
- Procedure: internal jugular venous cannulation
- type
- ACTIVE_COMPARATOR
- label
- transverse approach
- description
- cannulation will be transverse approach
- interventionNames
- Procedure: internal jugular venous cannulation
Primary outcomes (1)
- measure
- % of patients with successful cannulation in first attempt
- timeFrame
- at the procedure of cannulation
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 3 Years
- Maximum age
- 12 Years
Show eligibility criteria text
Inclusion Criteria: * patients age 3 months to 12 years old, weight 5-20 kg, male or female * who undergo heart surgery and indicated to have central venous cannulation * American Society of Anesthesiologist Physical Class 1-3 * Family or representation of the patients agreed to participate in this study and sign informed consent Exclusion Criteria: * history of surgery in the area of cannulation * already placed central venous cannulation \<72 hours in the same venous * sign of infection, hematoma, emphysema, in the area of cannulation * history of cervical trauma * severe hemostatic disorder (International Normalized Ratio\>2, thrombocyte \<50.000, Prothrombin time\>1.5 times, Activated Partial Thromboplastin Time \> 1.5 times
References
Publications (0)
Data not yet available
No reference posted for this study.