- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06862492
Open Surgical, Modified Seldinger's and US Techniques for Jugular Central Line Insertion in Infants
Comparing Open Surgical, Modified Seldinger's and Ultrasound Guided Techniques for Jugular Central Line Insertion in Infants
Study Overview
Status
Detailed Description
Central venous catheterization is an essential technique in the intensive care units , for the administration of life-saving treatments including total parenteral nutrition, nutritional support, and intravenous medication. The internal jugular vein is often chosen because of its relatively larger size than the subclavian vein, lower risk of complications, and easy compressibility in case of bleeding. To facilitate Central venous catheterization, ultrasound guidance over anatomical guidance in closed techniques has been introduced bringing increased success rates, decreased catheterization times, and reduced complications.
Open surgical insertion is a common method of tunneled catheter implantation in the past, but the percutaneous approach has recently gained more popularity . The modified Seldinger's insertion technique is a catheter over guide wire technique, based on the original Seldinger's technique, and has not been widely adopted in Intensive care units. However, the modified Seldinger's technique has been successfully introduced into Intensive care units, and it is now used as the only technique for peripherally inserted central venous catheter insertion .
Central venous catheterization have become a mandatory part of clinical management in a variety of clinical circumstances in pediatric age groups. It allows resuscitation for intravascular fluid depletion and access for vasoactive medications and antibiotics, and it provides a means for hemodynamic monitoring and pacing. US guided closed technique is the updated use for insertion of IJV catheterization because it can both increase the success rate and decrease the complications related to Central venous catheterization placement
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mohamed Amin, Demonstrator
- Phone Number: 0020 10 19848433
- Email: mohamed.salah.mms@gmail.com
Study Locations
-
-
-
Tanta, Egypt, 31527
- Tanta University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 1-patients needed Central venous catheterization insertion in the internal jugular vein for medical or surgical causes.
2- patients with age ranging from birth till two years
Exclusion Criteria:
- 1- femoral or subclavian Central venous catheterization insertion. 2- patients with thrombosed internal jugular vein . 3- patients with previous Central venous catheterization insertion. 4- those with malignant conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Open surgical technique group
included 35 patients underwent Central venous catheterization insertion using Open surgical technique group
|
The technique was performed following the descriptions of Farhadi et al. The infant was positioned in 30° (Trendelenburg's position), with a roll under his shoulders for neck extension and rotated to contralateral side of the surgical side to expose the incision site. Incision was done under sedation and pulse oximeter to monitor the oxygen saturation during the technique. Under complete aseptic technique, a small transverse incision 1cm was made on triangle bordered by the clavicle inferiorly and by the sternal and clavicular heads of the sternomastoid muscle medially and laterally. With blunt dissection we separate the two heads of the sternomastoid exposing the internal jugular vein . Then internal jugular vein cut down was performed and catheter inserted through it, all internal jugular vein venotomies were repaired as needed by 6/0 Polypropylene (Prolene®) suture and the wound was closed by absorbable polyglactin (Vicryl) suture |
|
Experimental: Modified Seldinger's technique group
included 35 patients underwent Central venous catheterization insertion
|
After proximal and distal control of the vein, a 24-G.
cannula was carefully inserted directly to the internal jugular vein .
The guidewire was inserted through the cannula, then the cannula was removed.
A size 4-5 French short length catheter was passed and brought out through the guidewire, then the guidewire was removed.
The wound was closed after the correct catheter position and good haemostasis was obtained; the area was covered with sterile dressing.
|
|
Experimental: Ultrasound guided Central venous catheterization insertion group
included 35 patients underwent closed ultrasound guided Central venous catheterization insertion
|
Ultrasound probe was connected to ultrasound unit and focused with ultrasonic gel and wrapped in a sterile plastic sheath.
By wrapping the transducer in a sterile sheath, the probe place perpendicular to the long axis of the vessel, standard US two-dimensional (2D) imaging was used to visualize the vein in the short-axis view as a circle.
Catheterization was performed under continuous dynamic observation of real-time 2D images.
Insertion needle was advanced through the skin under US guidance into the internal jugular vein .
A guidewire was then placed through the needle into the vein, and the needle was removed.
Then catheter was inserted over the wire into internal jugular vein .
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
success of cannulation
Time Frame: 20 minutes
|
Central venous cannulations in pediatric patients using each technique
|
20 minutes
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Technique time
Time Frame: within 30 minutes
|
within 30 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mohamed Amin, Demonstrator, Tanta University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 36264MS38/1/23
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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