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NCT06773325

Buzzy Application During Heel Blood Collection in the Newborn

Completed NA Last updated 14 January 2025
What this trial tests

NA trial testing Buzzy application in Buzzy in 80 participants. Completed in 30 November 2024.

Timeline
1 September 2024
Primary endpoint
20 November 2024
30 November 2024

Quick facts

Lead sponsorYuzuncu Yil University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposehealth services research
Enrollment80
Start date1 September 2024
Primary completion20 November 2024
Estimated completion30 November 2024
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Yuzuncu Yil University

Who can join

Adults 0 Days to 28 Days, any sex, with Buzzy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective The aim of this study was to evaluate the effects of Buzzy device application during heel prick blood collection on pain level and comfort in newborns. Method. The study was conducted in a Family Health Center affiliated to the Public Health Directorate of a province in eastern Turkey between September and November 2024 using a randomized controlled experimental design. The study sample consisted of 80 newborn infants born at 37-42 weeks gestational age and within the first 28 days of birth (Buzzy group: n = 40, control group: n = 40). The Buzzy group was treated by placing the Buzzy device approximately 30 seconds before heel prick blood collection. In the control group, routine heel prick was performed without any application. Neonatal introduction form, Neonatal Infant Pain Scale and Neonatal Comfort Behavior Scale were used for data collection.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Yuzuncu Yil University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06773325.

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