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Vein Imaging Device on First-Attempt Success in Peripheral Intravenous Catheter Insertion (Veinimaging)

D

Dokuz Eylül University (DEU)

Status

Completed

Conditions

Catheterization, Peripheral
Children
Catheter Complications
Pain
Catheters, Indwelling

Treatments

Device: Veinlite PEDI2

Study type

Interventional

Funder types

Other

Identifiers

NCT07006038
Vein Imaging-PED
578-SBKAEK (Registry Identifier)

Details and patient eligibility

About

This study aimed to evaluate the impact of vein visualization device on catheter placement success and catheter-related complications during peripheral IV catheter insertion in pediatric emergency departments. This randomized controlled trial compares the group using a vein visualization device with the group using the standard method.

Full description

There were two groups in this study: the vein imaging device and the control group.

The children to be included in this study consisted of pediatric patients who were admitted to the PED. There were two groups in this study: the vein imaging device and the control group. If the physician requested a peripheral intravenous catheter (PIC), the vein imaging device was applied to increase the first-attempt success of the PIC in one group. In addition, there was a control group in which any device was not used. One trained nurse who was a PhD student enrolled the participants who met the eligibility criteria.

The patients who were scheduled for PIC insertion were allocated to groups according to the randomization scheme. After providing information to the child and the parent, the investigator obtained consent from the parent, and the group assignment was determined. The patients in the control group did not receive any additional interventions and were observed during the PIC insertion after obtaining consent.

The PIC procedure time started when the tourniquet connected. In the vein imaging device and the control groups, communication with the child was maintained using the questions mentioned above during the procedure by the researcher nurse. When the phlebotomist nurse decided on the insertion site for the PIC, the PIC was attempted. If the PIC was inserted on the first attempt, the PIC procedure time stopped. If not, when the PIC was successfully inserted, the PIC procedure time was stopped. The PIC insertion time was recorded in minutes for successful PIC insertion. After the PIC insertion area was closed with dressing and the materials were collected, the child's pain was assessed by the PED nurse with the FLACC pain scale.

Complication signs and symptoms are monitored in the PIC area. If the PIC is to be removed for any reason, the reason and time of removal are recorded. PIC indwelling time was recorded. If it was removed due to a complication, the PIC area was followed up by grading with infiltration, extravasation, and phlebitis scales.

Enrollment

206 patients

Sex

All

Ages

1 month to 6 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The physician must inform them that PIC must be inserted to administer medication and fluids
  • The parent must voluntarily agree to participate in the study, consent form must be obtained from the parent

Exclusion criteria

  • The child presenting to the pediatric emergency department must be in shock or severely dehydrated, requiring urgent intervention
  • No need for PIC
  • Presence of a central venous catheter (since there will be no need for PIC)
  • Selection of the lower extremities for PIC placement (since they may experience more pain and complication)
  • Use of sedatives or analgesics before the PIC procedure (at least 4 hours before)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

206 participants in 2 patient groups

Vein imaging device group
Experimental group
Description:
the PIC insertion area was visualized with the help of the device by the nurse. The vein imaging device was used before the catheter insertion attempted to view the patient's veins.
Treatment:
Device: Veinlite PEDI2
Control group
No Intervention group
Description:
no vein imaging device was used before cathater insertion

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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