search
Back to results

Acupuncture for Preterm Infants Requiring Eye-exam (MAGNIFIC-ROP)

Primary Purpose

Retinopathy of Prematurity, Pain, Acupuncture

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Magnetic acupuncture
stickers (magnets removed)
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Retinopathy of Prematurity

Eligibility Criteria

29 Weeks - 36 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Infants weighing less than 1250g at birth admitted into the NICU at the Royal Alexandra Hospital will require routine,regularly scheduled ROP eye-exams beginning at 32 weeks corrected age. We will not enroll any infant who meets any exclusion criteria.

Exclusion Criteria:

  1. Chronic pain stimuli (e.g. infants who have had recent surgery)
  2. Neurological problems that could impair pain perception (e.g. diagnosis of intraventricular hemorrhages Grade III or greater)
  3. Cardiorespiratory problems that could impair oxygenation (e.g. any infant who is intubated and requiring mechanical ventilation)

Sites / Locations

  • University of Sydney
  • Royal Alexandra Hospital
  • University of Malaya Medical Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Intervention - Magnetic acupuncture

Control - Placebo control

Arm Description

Infants randomized to the intervention arm will have 5 magnetic stickers placed on both ears approximately 1 hour before the eye-exam and will stay in place for approximately 1 hour after the eye-exam. Total duration of study 2.5-3 hours

In this arm the infants will have 5 stickers (magnets removed) placed on their ear approximately 1 hour before the eye-exam and will stay in place for approximately 1 hour after the eye-exam. Total duration of study 2.5-3 hours

Outcomes

Primary Outcome Measures

Changes in Premature Infant Pain Profile (PIPP) scores
Mean pain scores on the Premature Infant Pain Profile (PIPP) scores

Secondary Outcome Measures

Heart rate changes
During eye-exam - which will take 5min (comparison between baseline before eye-exam and mean value during eye-exam)
Changes in oxygen saturation
During eye-exam - which will take 5min (comparison between baseline before eye-exam and mean value during eye-exam)
changes in cerebral oxygenation
During eye-exam - which will take 5min (comparison between baseline before eye-exam and mean value during eye-exam)

Full Information

First Posted
June 26, 2018
Last Updated
July 10, 2020
Sponsor
University of Alberta
search

1. Study Identification

Unique Protocol Identification Number
NCT03650621
Brief Title
Acupuncture for Preterm Infants Requiring Eye-exam
Acronym
MAGNIFIC-ROP
Official Title
Magnetic Non-Invasive Acupuncture For Infant Comfort A Pilot Study in Preterm Infants Requiring Eye-exam for Retinopathy of Prematurity
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
August 24, 2018 (Actual)
Primary Completion Date
September 30, 2019 (Actual)
Study Completion Date
April 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alberta

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose is to investigate whether non-invasive acupuncture - NIA (i.e. acupuncture without needles) will help reduce pain for babies in the Neonatal Intensive Care Unit (NICU) during their routine weekly eye-exam for Retinopathy of prematurity. Retinopathy of prematurity (ROP) is an eye disease most commonly affecting premature babies born weighing less than 1250 grams. Retinopathy of prematurity occurs because these premature babies require oxygen because of their immature lungs. The oxygen then stimulates the growth of blood vessels in the retina, causing the retina to be detached from the eye, which causes vision impairment. To examine if the vessels grow at the back of the eye, an eye-doctor visits bi-weekly once the baby is 32 weeks corrected age to assess if the blood vessels change. If there is a lot of growth, the eye-doctor would use a laser to treat the eye to prevent further growth. During the bi-weekly eye-exam, the premature infant receives sucrose (a type of sugar) for pain management. The investigator will assess pain a premature babies experience during this exam and found that there are extremely high scores of pain despite sucrose and the investigator believe this pain and stress caused by these procedures could be reduced by adding: Magnetic Acupuncture Also, untreated pain causes stress (lower oxygen levels, higher heart rates), discomfort and poorer long term outcomes. Finding the best treatment and prevention for the pain caused by procedures in the NICU is therefore extremely important for any baby.
Detailed Description
Background: Infants in neonatal intensive care units (NICU) may experience as many as 14 painful and stressful procedures every day. Even common and seemingly innocuous procedures like routine eye exams can cause relatively severe pain that is only marginally alleviated by powerful analgesics like morphine. Infants subject to severe and repeated episodes of pain are at risk of immediate and long-term sequelae, including intraventricular hemorrhage, impaired neurodevelopment, poor postnatal growth, cognitive and motor dysfunction and emotional dysregulation. Pharmacological analgesia is often used in the NICU to either prevent or alleviate procedural pain but none are completely effective and almost all have potentially detrimental side-effects. Non-pharmacological measures (e.g., kangaroo care and breastfeeding) are also used but these methods may not be feasible in very sick infants or if pain is extremely severe. Methods to provide safe and effective analgesia for babies in the NICU are therefore needed. Acupuncture has been used for thousands of years to prevent and treat pain and various health conditions. There are many forms of acupuncture, including needling, electrical currents, laser, and pressure, all of which aim to modulate activity of key nociceptive structures, neurotransmitter secretions and parasympathetic function. The investigator have reported about the safety and efficacy of auricular magnetic acupuncture (MA) in the NICU environment during heel pricks or neonatal withdrawal. One of the most common and painful procedure preterm infants experience during their NICU stay is their weekly eye-exam to assess for Retinopathy of Prematurity. Currently, during the eye exam infants receive sucrose for analgesia, which has very limited effects on pain release. The investigator propose to examine if using auricular MA will reduce pain during their eye-exam. Research question: Does auricular MA decrease pain in preterm infants compared to placebo with control. Aim: To determine if auricular MA will reduce pain compared to placebo with control in preterm infants during their eye exam. Hypothesis: The investigator hypotheses that auricular MA will reduce pain compared to placebo with control in preterm infants during their eye exam. Methods: Infants who will require their routine eye exam (beginning at 32 weeks corrected age) will be randomized to either auricular MA or auricular placebo/sucrose after parental informed consent. Five auricular MA or placebo stickers will be placed on acupuncture sites on both ears for 1 hour prior to the eye-exam by a non-blinded investigator. Pain responses will be assessed with the Premature Infant Pain Profile (PIPP) by blinded clinicians before, during and after each eye-exam. The study will be conducted in the NICU at the Royal Alexandra Hospital as a single-blinded randomized, placebo controlled study to investigate the safety and feasibility of using magnetic stickers in the NICU environment. The randomization sequence will be pre-specified, computer generated into block sizes of 2-4. Allocations will be concealed in sequential opaque envelopes stored in a secure location. A single unblinded investigator will complete randomization, administer the intervention, but will not be involved in data collection. Infants will be randomized to receive either MA or placebo stickers that are to be applied bilaterally to the 5 auricular acupuncture points as per the Battlefield Acupuncture (BFA) protocol at least 1 hour prior to the eye-exam by the unblinded investigator. Placebos will be constructed by removing the magnet ball from pre commercially-available MA plasters (Sakamura, Helio Acupuncture, Japan). The magnet site on placebo and magnetic stickers will then be concealed with a thick application of white, opaque correction fluid. Stickers will be removed 1 hour after the eye-exam. Sucrose for pain management can be given as per NICU policy. The ROP eye exams are performed by a dedicated group of five physicians therefore consistency will be maintained. Primary outcome: Infant's response to the pain during the eye-exam, measured by the PIPP score, a validated, quantitative pain assessment tool for use in premature infants. Expected outcomes: The proposed study aims to examine if auricular MA compared to placebo will decrease pain in premature infants. If validated, the results of the study could be translated into NICUs around the world and might benefit a large number of babies each year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Retinopathy of Prematurity, Pain, Acupuncture, Premature Infant

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
this is a 2-arm parallel design randomized controlled trial with 3 sites recruiting infants
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
patients are preterm infants and therefore mask, health care providers will be masked as well as outcome assessors.
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention - Magnetic acupuncture
Arm Type
Experimental
Arm Description
Infants randomized to the intervention arm will have 5 magnetic stickers placed on both ears approximately 1 hour before the eye-exam and will stay in place for approximately 1 hour after the eye-exam. Total duration of study 2.5-3 hours
Arm Title
Control - Placebo control
Arm Type
Placebo Comparator
Arm Description
In this arm the infants will have 5 stickers (magnets removed) placed on their ear approximately 1 hour before the eye-exam and will stay in place for approximately 1 hour after the eye-exam. Total duration of study 2.5-3 hours
Intervention Type
Device
Intervention Name(s)
Magnetic acupuncture
Intervention Description
5 magnetic acupuncture stickers will be placed on the infants ear
Intervention Type
Device
Intervention Name(s)
stickers (magnets removed)
Intervention Description
in this group 5 stickers (magnets removed) will be placed on the infants ear
Primary Outcome Measure Information:
Title
Changes in Premature Infant Pain Profile (PIPP) scores
Description
Mean pain scores on the Premature Infant Pain Profile (PIPP) scores
Time Frame
Comparison of baseline (= 1 hour before eye-exam) and after eye-exam (1 hour after)
Secondary Outcome Measure Information:
Title
Heart rate changes
Description
During eye-exam - which will take 5min (comparison between baseline before eye-exam and mean value during eye-exam)
Time Frame
changes in heart rate in beats per minute 1 hour before and 1 hour after eye-exam
Title
Changes in oxygen saturation
Description
During eye-exam - which will take 5min (comparison between baseline before eye-exam and mean value during eye-exam)
Time Frame
changes in oxygen saturation in % 1 hour before and 1 hour after eye-exam
Title
changes in cerebral oxygenation
Description
During eye-exam - which will take 5min (comparison between baseline before eye-exam and mean value during eye-exam)
Time Frame
changes in cerebral oxygenation % 1 hour before and 1 hour after eye-exam

10. Eligibility

Sex
All
Minimum Age & Unit of Time
29 Weeks
Maximum Age & Unit of Time
36 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants weighing less than 1250g at birth admitted into the NICU at the Royal Alexandra Hospital will require routine,regularly scheduled ROP eye-exams beginning at 32 weeks corrected age. We will not enroll any infant who meets any exclusion criteria. Exclusion Criteria: Chronic pain stimuli (e.g. infants who have had recent surgery) Neurological problems that could impair pain perception (e.g. diagnosis of intraventricular hemorrhages Grade III or greater) Cardiorespiratory problems that could impair oxygenation (e.g. any infant who is intubated and requiring mechanical ventilation)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Georg Schmolzer, MD, PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Sydney
City
Sydney
State/Province
New South Wales
Country
Australia
Facility Name
Royal Alexandra Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T5H 3V9
Country
Canada
Facility Name
University of Malaya Medical Centre
City
Kuala Lumpur
Country
Malaysia

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
once study has been completed
IPD Sharing Access Criteria
email to PI
Citations:
PubMed Identifier
33425820
Citation
Gan KML, Oei JL, Quah-Smith I, Kamar AA, Lordudass AAD, Liem KD, Lindrea KB, Daly M, Gaunker N, Mangat AK, Yaskina M, Schmolzer GM. Magnetic Non-invasive Auricular Acupuncture During Eye-Exam for Retinopathy of Prematurity in Preterm Infants: A Multicentre Randomized Controlled Trial. Front Pediatr. 2020 Dec 23;8:615008. doi: 10.3389/fped.2020.615008. eCollection 2020.
Results Reference
derived

Learn more about this trial

Acupuncture for Preterm Infants Requiring Eye-exam

We'll reach out to this number within 24 hrs