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Completed

NCT Number: NCT00519207

Evaluation of Topical Liposomal Lidocaine and Oral Sucrose for Treatment of Pain in Newborns Undergoing Venipuncture

The objective of this study is to determine the relative efficacy of sucrose, liposomal lidocaine, and sucrose plus liposomal lidocaine, on reducing pain during venipuncture in newborn infants.

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Key information

Age range

1 day–7 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Mount Sinai Hospital, Toronto, Ontario, Canada

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About this study

Despite the fact that modern medical practice is greatly advanced, pain is inflicted on all Canadian newborn infants in the first days and months of life from blood tests, injections and cannulations designed to prevent, diagnose or manage medical conditions. Procedural pain in newborn infants is a significant burden to infants, their parents, healthcare workers, and society at large.

This study proposes a large randomized controlled trial to determine the optimal analgesic regimen for procedural pain using methods that can be easily implemented in clinical practice. We will study liposomal lidocaine cream and sucrose oral liquid, used alone, or together, to manage procedural pain. Liposomal lidocaine is a relatively new anaesthetic formulation ideally suited for young infants due to the established role of lidocaine in neonatal clinical medicine. Sucrose (sugar water) reduces pain responses and is promoted in consensus guidelines developed by pain experts. However, it is perceived by many front-line clinicians to be simply a comforting agent rather than a true analgesic. Studying liposomal lidocaine and sucrose together is important since the combination may prove superior to either agent alone, and may even prevent or abolish pain from clinical procedures.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy newborn infants
  • ≥ 37 weeks gestational age.

Exclusion criteria

  • neonatal intensive care unit (NICU) admission
  • asphyxia, seizures
  • major birth defect (heart, brain, genetic syndrome)
  • circumcised during study
  • receiving analgesia/sedatives.

Treatment and study plan

Lidocaine

Drug

1g of liposomal lidocaine will be administered 30-40 minutes prior to venipuncture and occluded by a dressing.

Other names: Maxilene 4

24% Sucrose Solution

Drug

2ml of 24% sucrose will be administered 2 minutes prior to venipuncture

Other names: TootSweet

Primary outcomes

  1. Infant pain during venipuncture as assessed by facial grimacing response.

    Time frame: During venipuncture

Secondary outcomes

  1. Visual Analog Scale scores

    Time frame: During venipuncture

  2. Cry duration

    Time frame: During venipuncture

  3. Heart rate

    Time frame: During venipuncture

  4. Number of attempts until procedure completion

    Time frame: From first needle poke to completion

  5. Endomorphins-1,-2 levels

    Time frame: Before and 10 minutes after sucrose/sucrose placebo administration

  6. Procedure duration

    Time frame: From first needle poke to completion

  7. Lidocaine levels

    Time frame: 5-15 minutes after the study cream is removed

Sponsors and collaborators

Lead sponsor

The Hospital for Sick Children

Other

Collaborators

  • Canadian Institutes of Health Research (CIHR)

Registry information

Official study title

Evaluation of Topical Liposomal Lidocaine and Oral Sucrose for Treatment of Pain in Newborn Infants Undergoing Venipuncture: A Randomized Controlled Trial

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Aug 22, 2007
Registry last updated
Jul 19, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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