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CompletedNCT02214589Updated Mar 13, 2020

Non-pharmacological Interventions for Procedural Pain in Premature Neonates

An interventional study of Oral glucose, facilitated tucking, NNS and Oral glucose and NNS in Prevention of Procedural Pain, Reduction of Procedural Pain and Biochemical Effects of Oral Dextrose, sponsored by Loma Linda University. Completed at 1 site in United States. Open to participants aged Up to 1 Month. Per ClinicalTrials.gov, last updated 2020-03-13.

Sponsored by Loma Linda University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
203
Allocation
Randomized
Ages
Up to 1 Month
Sex
All
01

Study summary

A. Specific Aims Premature infants admitted to the neonatal intensive care unit (NICU) require up to several hundred procedures during their hospitalization. Many of these are tissue-damaging procedures (TDPs) known to cause pain [1]. Through funding from NINR, the investigators found that TDPs not only caused pain but also increased markers of ATP degradation and oxidative stress[2[. The TDP was tape removal, a commonly performed procedure in the NICU2.

Based on this finding, the investigators sought to determine if interventions that relieve pain also reduce biochemical markers of ATP degradation and oxidative stress. The investigators first examined the effect of oral sucrose, a commonly used intervention, when given before a heel lance. The investigators chose heel lance because it is the most predominant painful procedure in the NICU, as shown in 29 different clinical trials[3]. The investigators hypothesized that since oral sucrose is documented to significantly reduce pain scores, then administration of this analgesic will also decrease markers of ATP degradation and oxidative stress. However,the investigators observed the opposite effect. Although a single dose of oral sucrose reduced behavioral markers of pain, it significantly increased biochemical markers of ATP degradation (hypoxanthine, uric acid) and oxidative stress (allantoin) over time[4]. More importantly, the effect of oral sucrose on breakdown markers of ATP were enhanced and were significantly higher in neonates that were intubated or were receiving more than 30% FiO25. These findings lead to the question: If oral sucrose does not effectively reduce the biochemical effects of procedural pain, what intervention or groups of intervention will decrease both behavioral markers of procedural pain and reduce ATP utilization and oxidative stress in premature neonates? For this RO1 renewal, the investigators propose to test the individual and additive effects of two commonly used interventions for procedural pain. These interventions are (a) administration of 30% oral glucose and non-nutritive sucking (NNS) (b) facilitated tucking and NNS c) administration of 30% oral glucose, facilitated tucking and NNS. Administration of 30% oral glucose was documented to decreased procedural pain scores[6-9] without the potential adverse effects of fructose, a key ingredient of sucrose[10-11]. Facilitated tucking is the gentle positioning of preterm infants with arms and legs in a flexed, midline position close to the body, while either in a side-lying or prone position[12]. Because tachycardia often accompanies pain, a documented benefit of facilitated tucking is stabilization of heart rate and reduction of motor activity (flailing)[12-13]. Non-nutritive sucking refers to the provision of a weight-appropriate pacifier[14]. The painful procedure will be a clinically required heel lance, which refers to the puncture of a newborn's heel for blood glucose using a specially designed lancet. Our general hypothesis is that commonly used clinical interventions known to reduce procedural pain alter biochemical markers of ATP degradation, oxidative stress and cell injury.

Specific Aim 1 will determine whether (a) 30% oral glucose and NNS or (b) facilitated tucking and NNS or (c) 30% oral glucose with facilitated tucking and NNS will decrease procedural pain.

  • Pain will be quantified using a validated pain scoring tool, the Premature Infant Pain Profile (PIPP). Individual and additive effect of interventions will be determined.

Specific Aim 2 will determine whether (a) 30% oral glucose and NNS or (b) facilitated tucking and NNS or (c) 30% oral glucose with facilitated tucking and NNS will decrease biochemical markers of ATP degradation, oxidative stress and oxidative cell injury.

  • Products of ATP breakdown in plasma-hypoxanthine (Hx), xanthine (Xa), and uric acid (UA)-will be measured using high performance liquid chromatography.
  • Oxidative stress will be quantified by measuring plasma levels of allantoin using mass spectrometry.
  • Cell injury will be quantified by measuring plasma levels of F2 isoprostane using liquid-chromatography/mass spectrometry.
02

Conditions studied

  • Prevention of Procedural Pain
  • Reduction of Procedural Pain
  • Biochemical Effects of Oral Dextrose
03

In context

Premature Birth

2,554 studies on the registry are indexed under Premature Birth; 498 are open to participants now.

This study's enrollment of 203 is above the median of 84 across 1,689 interventional studies indexed under Premature Birth.

Browse Premature Birth studies →

Lead sponsor

Loma Linda University is the lead sponsor of 297 studies on the registry; 48 are open to participants now.

Of its 28 completed or terminated interventional studies of FDA-regulated products, 23 (82%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 1 Month
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Potential subjects are premature infants between 28-36 weeks gestation, have an arterial or central catheter in place and have a clinically required heel lance.

Exclusion criteria

Exclusion Criteria:

  • Requirement for surgery
  • Intraventricular hemorrhage (IVH) ≥ grade 3
  • Neonates on medications such as morphine, fentanyl, versed, muscle relaxants, phenobarbital, or dilantin
  • Renal injury (plasma creatinine > 1 mg/dl)
  • Severe cyanotic heart disease or severe respiratory distress
  • Chromosomal anomaly
  • Facial anomaly
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Single group
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
203 participants (actual)

Study arms

  • Active comparator
    Oral glucose and NNS

    Oral glucose and NNS

    Other: Oral glucose and NNS

  • Active comparator
    Oral glucose and facilitated tucking and NNS

    Oral glucose, facilitated tucking and NNS

    Other: Oral glucose, facilitated tucking, NNS

  • Active comparator
    Facilitated Tucking and NNS

    Facilitated tucking and NNS

    Other: Facilitated tucking and NNS

Interventions

  • OtherOral glucose, facilitated tucking, NNS
  • OtherOral glucose and NNS
  • OtherFacilitated tucking and NNS
06

What researchers measure

Primary outcomes

  1. Decreased pain score using the Premature Infant Pain Profile pain scoring tool

    A decrease in pain score will be quantified using the validated tool Premature Infant Pain Profile, which will be scored by a neonatologist blinded to group assignment.

    Time frame: at time of heelstick

07

Study locations

1 site
  • Loma Linda University Children's Hospital
    Loma Linda, California 92354, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 13, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02214589
Lead sponsor
Loma Linda University
Responsible party
Danilyn Angeles, PhD (Professor, Loma Linda University) — Principal investigator
First posted
Aug 12, 2014
Start date
Aug 2014
Primary completion
Dec 2019
Completion
Dec 2019
Last update
Mar 13, 2020

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2020. You cannot join it, but the record below documents what was studied.

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