Ultrasound Guided Supraclavicular and Infraclavicular Subclavian vs Catheterization in Pediatric
NCT ID: NCT06575491
Last Updated: 2024-08-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
40 participants
INTERVENTIONAL
2023-09-01
2024-06-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Short-axis/out-of-plane Approach Versus Oblique- Axis Approach for US Guided IJV Catheterization in Infants.
NCT06652490
Efficacy of Ultrasound-guided Internal Jugular Vein Versus Supraclavicular Subclavian Vein Cannulation in Neonates and Infants Less Than 5 kg.
NCT05956028
Right Versus Left Distal Axillary Approach For Subclavian Vein Cannulation
NCT06761326
Ultrasound Guided Axillary Venous Cannulation in Pediatrics
NCT02806401
Standard Ultrasound Guidance vs. New Needle-steering Device in Subclavian Venous Catheterization
NCT06050902
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Central venous catheter (CVC) placement is one of the most important invasive procedures in the intensive care for children of all ages. And health care outcomes largely depend on the success of its implementation. There are a large number of historically and clinically significant methods of central venous catheterization, and the advantages and disadvantages of each of them have been discussed for many years.
Ultrasonography is becoming an increasingly useful adjunct in the placement of Percutaneous central lines.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Supraclavicular group
Patients submitted to Supraclavicular approach for ultrasound-guided Subclavian veinous catheterization.
Ultrasound-guided supraclavicular approach
Patients submitted to Supraclavicular approach for ultrasound-guided Subclavian veinous catheterization.
Infraclavicular group
Patients submitted to Infraclavicular approach for ultrasound-guided Subclavian veinous catheterization.
Ultrasound-guided infraclavicular approach
Patients submitted to Infraclavicular approach for ultrasound-guided Subclavian veinous catheterization.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Ultrasound-guided supraclavicular approach
Patients submitted to Supraclavicular approach for ultrasound-guided Subclavian veinous catheterization.
Ultrasound-guided infraclavicular approach
Patients submitted to Infraclavicular approach for ultrasound-guided Subclavian veinous catheterization.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Both sexes.
* All children who need central venous line insertion.
* Intra-operative Hemodynamic monitoring.
* Volume and Inotrope Resuscitation.
* Difficult Peripheral IV Access.
* Intravenous Nutrition and Medications.
Exclusion Criteria
* Distorted anatomy.
* Infection systemic or cutaneous near the proposed Point of insertion.
* Skeletal deformity.
* History of previous neck surgery.
* Head and neck mass.
* Guardian Refusal.
* Pneumothorax Or Hemothorax.
4 Years
12 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Al-Azhar University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Radi Mohamed Radi Mostafa
Resident of Anesthesiology, Surgical Intensive Care, Faculty of Medicine, Al-Azhar University, Cairo, Egypt.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Al-Azhar University
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
0377/2023
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.