AccuVein AV400 Device Versus Ultrasound-guided Cannulation of the Great Saphenous Vein at the Ankle in Infants
NCT ID: NCT04164862
Last Updated: 2019-11-15
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
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UNKNOWN
NA
100 participants
INTERVENTIONAL
2019-09-01
2020-01-31
Brief Summary
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Most peripheral veins in infants are too superficial and too small for direct visualization. A promising alternative approach could be the great saphenous vein (GSV) at the level of the medial malleolus due to the adequate diameter and the relatively deep position relative to the skin.
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Detailed Description
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Patient and method:
A prospective, randomized study will be conducted from May 2019 till November 2019; at least 50 patients will be allocated in each group; at the Alexandria Main University Hospital after approval of the Medical Ethics Committee. Informed written consent will be obtained from the patient's parents. Infants' ≤12 months with ASA physical status I and II, undergoing elective surgery with no visible veins at the dorsum of the hands or feet will be enrolled in the study. Infants will be randomly assigned, by using a block of four randomization provided by www.randomization.com, into two groups; an AV400 group (using the AccuVein AV400 for peripheral venous insertion) and a ultrasound guided group (using the ultrasound for peripheral venous insertion). The performers of cannulation will be done by expert anesthetists, having a minimum of 5 times experience in ultra sound guided IV cannula insertion and with the AccuVein AV400 device.
Preoperatively in all infants, both medial malleolar areas will be prepared with EMLA cream , premedication with 1 mg/ kg rectal midazolam (maximum dose 15 mg) will be done at 30 minutes preoperative. Establishment of standard monitoring (SpO2, ECG, non-invasive arterial pressure) and then induction of general anaesthesia will be done via a face mask with sevoflurane FIO2 40% - O2/air and after successful induction of general anaesthesia, the EMLA tapes will be removed .Assisted ventilation via the face mask will be done until establishment of venous access either through using Acc Vein AV400 or through ultrasound guided for the great saphenous vein. On each occasion, the observer will record the time of tourniquet application, the time of successful cannulation or four skin punctures, and the number of cannulation attempts. A cannulation attempt will be defined as any backward and forward movements of the needle, regardless of whether the needle was out of the skin. Successful cannulation will be defined by the absence of tissue swelling around the puncture point after injection of 5 ml of crystalloid solution. In both groups, a maximal number of three attempts for establishment of venous access in one GSV will be performed. If the third attempt failed, the contralateral GSV will be punctured. If successful establishment of venous access in the contralateral GSV failed, the case will be counted as failure. In these cases, the external jugular vein will be used as an alternative approach for venous access. After successful establishment of venous access, the anaesthetic procedure will be continued depending on surgical requirements. Twenty-four hours after establishment of the venous access, the puncture site will be evaluated to detect possible haematoma or local infection.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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use ACCUVEIN AV400
Device to facilitate cannulation of the great saphenous vein at the ankle in infants
AccuVein AV400 Device Versus Ultrasound-guided Cannulation
Accuvein AV400 device versus Ultrasound guided cannulation
ULTRASOUND GUIDED CANNULATION
Ultrasound cannulation of the great saphenous vein in infants
AccuVein AV400 Device Versus Ultrasound-guided Cannulation
Accuvein AV400 device versus Ultrasound guided cannulation
Interventions
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AccuVein AV400 Device Versus Ultrasound-guided Cannulation
Accuvein AV400 device versus Ultrasound guided cannulation
Eligibility Criteria
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Inclusion Criteria
* ASA physical status I and II
* undergoing elective surgery
* with no visible veins at the dorsum of the hands or feet
Exclusion Criteria
ALL
Yes
Sponsors
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Alexandria University
OTHER
Responsible Party
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rehab zayed
Assistant Professor of Aneasthesia
Principal Investigators
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Rehab Zayed, Ass.Prof.
Role: PRINCIPAL_INVESTIGATOR
Alexandria University
yasser Osman, Ass. Prof.
Role: PRINCIPAL_INVESTIGATOR
Alexandria University
Locations
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Rehab A.Zayed
Alexandria, , Egypt
Countries
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Other Identifiers
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00018699
Identifier Type: OTHER
Identifier Source: secondary_id
00012098
Identifier Type: -
Identifier Source: org_study_id
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