Heel Lance Procedures

2

Review clinical trials related to Heel Lance Procedures. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Non-Pharmacological Methods in Heel Lance

This randomized controlled study was designed to compare the effects of Warm Foot Bath, ShotBlocker®, and Buzzy®-applied prior to heel lance-on the vital signs of newborns. Heel lance is one of the most frequently performed invasive procedures during the neonatal period, and the pain and stress experienced during the procedure may lead to alterations in vital parameters such as heart rate, respiratory rate, and oxygen saturation. Therefore, identifying non-pharmacological, safe, and feasible pain management methods is essential for enhancing the quality of nursing care. Data will be collected at three time points: before, during, and after the procedure, and changes in heart rate, respiratory rate, and SpO₂ will be recorded. With parental consent, the procedure will be video-recorded before, during, and after heel lance; the recordings will be anonymized and shared with experts for pain assessment. Additionally, the infant's crying duration and time to bleeding cessation will also be evaluated.

Participants needed: 90
Trial details
Age: 4-1Biological sex: AllType: InterventionalSponsor: Atlas UniversityUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Newborns with a gestational age of ≥37 weeks [+7]

Preterm or low birth weight infants (< 2500 g) [+2]

Status: Not yet recruiting

The Effect of Su Jok Therapy on Pain During Heel LanceProcedure in Newborn

Objective: To determine the effect of Su Jok therapy on pain levels during the heel lance procedure in newborns. The study will be conducted as a randomized controlled experimental trial with a pretest-posttest control group design. The heel lance procedure will be video recorded, and pain assessment will be performed independently by an experienced neonatal intensive care nurse with 7 years of clinical expertise and a neonatologist, using validated pain assessment scales.

Participants needed: 66
Trial details
Age: 1-1Biological sex: AllType: InterventionalSponsor: Ataturk UniversityUpdated: Sep 18, 2025Locations: 1
Eligibility criteria

Term newborns (≥37 gestational weeks) [+5]

Clinically unstable infants before or during the procedure (e.g., respiratory di... [+4]