Analgesic Effect of Oral 25% Glucose Versus Oral 24% Sucrose for Pain Relief During Heel Lance in Preterm Neonates
Primary Purpose
Pain
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Sucrose
Glucose
Sponsored by

About this trial
This is an interventional treatment trial for Pain focused on measuring Pain, Preterm, Neonates, 24% Sucrose, 25% Dextrose
Eligibility Criteria
Inclusion Criteria:
- Infants born at <37 weeks of gestational age
- Infants within first 48 hours of post natal life
- Infants having clinical indication for blood sampling
- Parental consent
Exclusion Criteria:
- Infants born with perinatal asphyxia, birth trauma, cardiorespiratory instability
- Infants with 5min APGAR score <7
- Infants having any syndromes, congenital anomalies or previous surgery
- Infants born to mothers known to be receiving opiates
- Infants administered muscle relaxants, sedatives & analgesics
- Infants born under general anesthesia
Sites / Locations
- Lady Hardinge Medical College
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Sucrose
Glucose
Arm Description
1ml of 24%sucrose will be administered prior to heel lance
1ml of 25% glucose will be administered prior to heel lance
Outcomes
Primary Outcome Measures
Painful response
Premature Infant Pain Profile(PIPP)
Secondary Outcome Measures
Duration of Crying
Duration of crying will be taken as the time between the first crying sound till total silence
Full Information
NCT ID
NCT01931020
First Posted
August 21, 2013
Last Updated
June 24, 2016
Sponsor
Lady Hardinge Medical College
1. Study Identification
Unique Protocol Identification Number
NCT01931020
Brief Title
Analgesic Effect of Oral 25% Glucose Versus Oral 24% Sucrose for Pain Relief During Heel Lance in Preterm Neonates
Official Title
Double Blind Randomised Controlled Trial to Compare the Efficacy of Oral 25% Glucose With Oral 24% Sucrose for Pain Relief During Heel Lance in Preterm Neonates
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
July 2014 (Actual)
Study Completion Date
July 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lady Hardinge Medical College
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
RESEARCH HYPOTHESIS-In preterm neonates during heel lance oral 25% glucose is more efficacious in reducing pain as compared to oral 24% sucrose when assessed by PIPP(Premature infant pain profile)
Detailed Description
Pain is "an unpleasant sensory and emotional experience associated with actual or potential tissue damage". Evaluation of pain in neonates is difficult due to the subjective nature of pain and the inability of neonates to verbally express pain. Surrogate measures used to describe pain in neonates include motor responses, facial expressions, cry and changes in physiologic parameters like heart rate, blood pressure, oxygen saturation and respiratory rate. Various changes have been compiled to create various scores. Validated scores for the assessment of pain include Neonatal Facial Coding System, Neonatal Infant Pain Scale or Premature Infant Pain Profile. These reactions to pain may contribute to the development of hypoxia, hypercarbia, acidosis, ventilator asynchrony, pneumothoraces, reperfusion injury and venous congestion and subsequent late intraventricular hemorrhage (IVH) or late extension of early intraventricular hemorrhage and periventricular leukomalacia. These behavioral changes may also disrupt postnatal adaptation, parent-infant bonding and feeding schedules.
Newborn infants routinely undergo painful invasive procedures, even after uncomplicated birth. Evidence shows that neonates do feel pain and may even have increased sensitivity to pain and to its long term effects compared with older infants. Treating procedural pain has become a crucial part of neonatal care. In healthy infants, the most common painful procedures are heel lance and venipuncture. Though minimally invasive, lancing is a painful procedure that activates cortical areas in brain .Repetitive procedural pain can lead to changes in the pain sensitivity threshold therefore, adequate analgesic control is needed. Pharmacological treatments are rarely used during these procedures because of concerns about their effectiveness (topical local anesthetics or paracetamol for heel pricks) and potential adverse effects (central analgesics). Therefore, non-pharmacological interventions are valuable alternatives. Recent interventions such as sweet oral solutions (sucrose or glucose) and non-nutritive sucking have been used frequently to alleviate pain.
Use of sucrose in preterm neonates has been advocated uniformly for pain relief. However, recently few reports have raised concerns over its safety and effect on neurodevelopment. Glucose has been used in pain relief in neonates but its therapeutic efficacy in comparison to oral sucrose in direct adequately powered RCT with pain assessment tools has not been evaluated in the Indian subcontinent. The present study was planned to evaluate the efficacy of 25% glucose solution with 24% sucrose solution for analgesia during heel lance in preterm neonates.
LACUNAE IN EXISTING KNOWLEDGE Existing literature on efficacy of glucose vs. sucrose is inconclusive on superiority of either. When a Medline search was carried out it returned limited results and no results returned from the Indian subcontinent which compared the two solutions using a multidimensional pain assessment tool. There is a need for an efficacious and cheap substitute which is readily available in NICU settings and sterile. Hence, the role of 25% Glucose in neonatal pain relief and safety associated with its use needs to be evaluated.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain
Keywords
Pain, Preterm, Neonates, 24% Sucrose, 25% Dextrose
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
94 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sucrose
Arm Type
Active Comparator
Arm Description
1ml of 24%sucrose will be administered prior to heel lance
Arm Title
Glucose
Arm Type
Experimental
Arm Description
1ml of 25% glucose will be administered prior to heel lance
Intervention Type
Drug
Intervention Name(s)
Sucrose
Other Intervention Name(s)
24% Sucrose
Intervention Description
The enrolled neonates will be administered 1ml of 24% sucrose. After 2 minutes heel lancing will be performed after cleaning the heel of neonate with a sterile spirit swab, with an auto lancet. Neonate's faces and monitor screen will be filmed in real time by using two independent video cameras during the entire procedure i.e. staring 2 minutes prior to heel lance and continue 2 minutes after the procedure. The PIPP will be assessed at 30 seconds, 1 minute and 2 minute after the procedure.
Intervention Type
Drug
Intervention Name(s)
Glucose
Other Intervention Name(s)
25% Glucose
Intervention Description
The enrolled neonates will be administered 1ml of 25% gluose. After 2 minutes heel lancing will be performed after cleaning the heel of neonate with a sterile spirit swab, with an auto lancet. Neonate's faces and monitor screen will be filmed in real time by using two independent video cameras during the entire procedure i.e. staring 2 minutes prior to heel lance and continue 2 minutes after the procedure. The PIPP will be assessed at 30 seconds, 1 minute and 2 minute after the procedure.
Primary Outcome Measure Information:
Title
Painful response
Description
Premature Infant Pain Profile(PIPP)
Time Frame
30 seconds after heel lance
Secondary Outcome Measure Information:
Title
Duration of Crying
Description
Duration of crying will be taken as the time between the first crying sound till total silence
Time Frame
Within 2 minutes following the procedure
Other Pre-specified Outcome Measures:
Title
Number of Participants with Adverse Events
Description
Choking, coughing or vomiting
Sustained tachycardia (HR>200) for >15 seconds
Sustained bradycardia (HR<80) for >15 seconds
Sustained tachypnea (RR>80) for >15 seconds
Sustained dyspnea (RR<20) for >15 seconds
Sustained oxygen desaturation <80% for >15 seconds
Time Frame
Within 2 minutes following the procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
34 Weeks
Maximum Age & Unit of Time
37 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Infants born at <37 weeks of gestational age
Infants within first 48 hours of post natal life
Infants having clinical indication for blood sampling
Parental consent
Exclusion Criteria:
Infants born with perinatal asphyxia, birth trauma, cardiorespiratory instability
Infants with 5min APGAR score <7
Infants having any syndromes, congenital anomalies or previous surgery
Infants born to mothers known to be receiving opiates
Infants administered muscle relaxants, sedatives & analgesics
Infants born under general anesthesia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vikram Datta, MD
Organizational Affiliation
Lady Hardinge Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lady Hardinge Medical College
City
New Delhi
State/Province
Delhi1
ZIP/Postal Code
110001
Country
India
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Analgesic Effect of Oral 25% Glucose Versus Oral 24% Sucrose for Pain Relief During Heel Lance in Preterm Neonates
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