search
Back to results

Treatment of Neonatal Jaundice With Filtered Sunlight Phototherapy: Safety and Efficacy in African Neonates

Primary Purpose

Jaundice, Neonatal

Status
Completed
Phase
Not Applicable
Locations
Nigeria
Study Type
Interventional
Intervention
Filtered-sunlight phototherapy
Conventional phototherapy
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Jaundice, Neonatal focused on measuring Hyperbilirubinemia, Neonatal

Eligibility Criteria

undefined - 14 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Subjects will be eligible to participate in the study if all of the following conditions exist:

  1. At time of birth, infant is > 35 weeks gestation (or > 2.2 kg if gestational age is not available
  2. Infant is < 14 days old at the time of enrollment
  3. At time of enrollment, infant has an elevated TcB defined as 3 mg/dL below the level recommended for high-risk infants per AAP guidelines or higher
  4. Parent or guardian has given consent for the infant to participate

Exclusion Criteria:

Subjects will be excluded from participation in the study if any of the following conditions exist at the time of enrollment:

  1. Infants with a condition requiring referral for treatment not available at the hospital study site and/or conventional phototherapy unit.
  2. Infants with a life-expectancy of < 24 hours
  3. Infants requiring oxygen therapy
  4. Infants clinically dehydrated or sunburned
  5. Infants with a temperature < 35.5 or > 38 degrees Centigrade
  6. Infants with ABE on clinical exam
  7. Infants meeting the criteria for EBT

Sites / Locations

  • Island Maternity Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Filtered-sunlight phototherapy

Conventional phototherapy

Arm Description

Infants will receive six hours per day of filtered-sunlight phototherapy for 1 to 10 days. The filtering will be done using window tinting film. Window tinting films by Solutia, Inc., and V-KOOL, Inc.

Infants will receive six hours per day of conventional phototherapy for 1 to 10 days.

Outcomes

Primary Outcome Measures

Safety of Phototherapy
For a given treatment day, the phototherapy treatment was deemed safe if that infant on that day did not have to be withdrawn from treatment due to hypo- or hyperthermia, sunburn or dehydration. Therefore safety is reported as a percentage of the total treatment days (i.e. number of safe treatment days divided by total number of treatment days).
Efficacy of Phototherapy
For a given evaluable treatment day, the phototherapy treatment was deemed effective if that infant on that day had a decrease in serum bilirubin level or (if <72hrs old) an rate of increase of less than 0.2 mg/dL/h. Therefore efficacy is reported as a percentage of the evaluable treatment days (i.e. number of effective evaluable treatment days divided by total number of evaluable treatment days).

Secondary Outcome Measures

Number of Participants Requiring Exchange Blood Transfusion
Exchange blood transfusion required to lower the bilirubin level. Serum bilirubin will be measured twice daily during filtered sunlight or conventional phototherapy exposure, for an expected average of four days, and a maximum of ten days.

Full Information

First Posted
August 30, 2011
Last Updated
January 31, 2019
Sponsor
University of Minnesota
Collaborators
Thrasher Research Fund
search

1. Study Identification

Unique Protocol Identification Number
NCT01434810
Brief Title
Treatment of Neonatal Jaundice With Filtered Sunlight Phototherapy: Safety and Efficacy in African Neonates
Official Title
Treatment of Neonatal Jaundice With Filtered Sunlight Phototherapy: Safety and Efficacy in African Neonates
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
Thrasher Research Fund

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary objective of this study is to determine the safety and efficacy of filtered sunlight phototherapy. Sunlight will be filtered by flexible (window-tinting) film. The subject population will be neonates born at Island Maternity Hospital, Lagos, Nigeria. The rationale for conducting the study is that in Nigeria, and other countries that may not have effective commercial light devices or have reliable access to electric power to operate them, filtered sunlight phototherapy might offer a safe and effective treatment for neonatal jaundice. Phase I of the study focused on the safety and efficacy of filtered sunlight phototherapy. Phase II of the study was a randomized controlled non-inferiority clinical trial comparing the efficacy of filtered sunlight phototherapy with conventional phototherapy.
Detailed Description
Numerous studies from resource-limited countries suggest that severe neonatal jaundice (NNJ) represents the largest unrecognized cause of neonatal morbidity and mortality in the world. Several studies from Africa rank jaundice as a leading cause of death in newborn nurseries. In Nigeria, Owa and Osinaike reported that jaundice (14%) was the second leading cause of death, while Ugwu et al, found that mortality from severe jaundice was comparable to birth asphyxia but greater than sepsis in neonates >24 hrs old to 7 days old. In Kenya, English et al reported NNJ as the third leading cause of both newborn admissions and deaths. Studies from Nigeria, Zimbabwe, Turkey, North Vietnam, Oman, and India listed acute bilirubin encephalopathy (ABE) and/or severe NNJ as a significant cause of morbidity, many of whom required exchange blood transfusion (EBT) in their nurseries. Unfortunately, phototherapy, as important as it is, may not be available to many infants with NNJ in these countries because of the lack of devices and/or of unreliable electrical power supply. Commercial phototherapy (PT) devices are expensive, often break down due to surges in electrical power, and are difficult to maintain due to unavailability of spare parts. Even where PT devices are available, most hospitals in these countries lack the resources to replace the fluorescent light bulbs at the recommended 2000-3000 hrs of use and simply leave ineffective tubes in place until they burn out. Moreover, very few hospitals have appropriate irradiance meters for monitoring the intensity of the blue light emitted by the lamps. In a recent study in Nigeria by Owa et al, none of the tested PT devices provided the level of irradiance required for intensive PT. Often, the only treatment a healthcare provider can suggest to the parents/guardians of jaundiced infants is to place their babies in sunlight. However, this practice is unsuitable due to several safety concerns. For instance, exposure to ultraviolet (UV) light may cause sunburn, while infrared (IR) light may cause the body to overheat. Moreover, the infant may lose body heat from the uncovered skin during treatment, with potential for dehydration. A safer, yet practical and economical, solution is needed, providing the basis for our proposal of filtered sunlight PT. The primary aims of this study were safety, efficacy and non-inferiority of filtered sunlight phototherapy compared to conventional phototherapy. Phase I of the study focused on the safety and efficacy of filtered sunlight phototherapy. Phase II focused on non-inferiority of efficacy as compared to conventional phototherapy while continuing to evaluate safety.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Jaundice, Neonatal
Keywords
Hyperbilirubinemia, Neonatal

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Non-inferiority trial comparing the two methods of phototherapy
Masking
None (Open Label)
Allocation
Randomized
Enrollment
447 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Filtered-sunlight phototherapy
Arm Type
Experimental
Arm Description
Infants will receive six hours per day of filtered-sunlight phototherapy for 1 to 10 days. The filtering will be done using window tinting film. Window tinting films by Solutia, Inc., and V-KOOL, Inc.
Arm Title
Conventional phototherapy
Arm Type
Active Comparator
Arm Description
Infants will receive six hours per day of conventional phototherapy for 1 to 10 days.
Intervention Type
Device
Intervention Name(s)
Filtered-sunlight phototherapy
Intervention Description
Infants will receive six hours per day of filtered-sunlight phototherapy for 1 to 10 days. The filtering will be done using window tinting film. Window tinting films by Solutia, Inc., and V-KOOL, Inc.
Intervention Type
Device
Intervention Name(s)
Conventional phototherapy
Intervention Description
Infants will receive six hours per day of conventional phototherapy for 1 to 10 days.
Primary Outcome Measure Information:
Title
Safety of Phototherapy
Description
For a given treatment day, the phototherapy treatment was deemed safe if that infant on that day did not have to be withdrawn from treatment due to hypo- or hyperthermia, sunburn or dehydration. Therefore safety is reported as a percentage of the total treatment days (i.e. number of safe treatment days divided by total number of treatment days).
Time Frame
Four to ten days
Title
Efficacy of Phototherapy
Description
For a given evaluable treatment day, the phototherapy treatment was deemed effective if that infant on that day had a decrease in serum bilirubin level or (if <72hrs old) an rate of increase of less than 0.2 mg/dL/h. Therefore efficacy is reported as a percentage of the evaluable treatment days (i.e. number of effective evaluable treatment days divided by total number of evaluable treatment days).
Time Frame
Four to ten days
Secondary Outcome Measure Information:
Title
Number of Participants Requiring Exchange Blood Transfusion
Description
Exchange blood transfusion required to lower the bilirubin level. Serum bilirubin will be measured twice daily during filtered sunlight or conventional phototherapy exposure, for an expected average of four days, and a maximum of ten days.
Time Frame
Four to ten days

10. Eligibility

Sex
All
Maximum Age & Unit of Time
14 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects will be eligible to participate in the study if all of the following conditions exist: At time of birth, infant is > 35 weeks gestation (or > 2.2 kg if gestational age is not available Infant is < 14 days old at the time of enrollment At time of enrollment, infant has an elevated TcB defined as 3 mg/dL below the level recommended for high-risk infants per AAP guidelines or higher Parent or guardian has given consent for the infant to participate Exclusion Criteria: Subjects will be excluded from participation in the study if any of the following conditions exist at the time of enrollment: Infants with a condition requiring referral for treatment not available at the hospital study site and/or conventional phototherapy unit. Infants with a life-expectancy of < 24 hours Infants requiring oxygen therapy Infants clinically dehydrated or sunburned Infants with a temperature < 35.5 or > 38 degrees Centigrade Infants with ABE on clinical exam Infants meeting the criteria for EBT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tina M Slusher, MD
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
Island Maternity Hospital
City
Lagos
Country
Nigeria

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26376136
Citation
Slusher TM, Olusanya BO, Vreman HJ, Brearley AM, Vaucher YE, Lund TC, Wong RJ, Emokpae AA, Stevenson DK. A Randomized Trial of Phototherapy with Filtered Sunlight in African Neonates. N Engl J Med. 2015 Sep 17;373(12):1115-24. doi: 10.1056/NEJMoa1501074.
Results Reference
derived
PubMed Identifier
24373547
Citation
Slusher TM, Olusanya BO, Vreman HJ, Wong RJ, Brearley AM, Vaucher YE, Stevenson DK. Treatment of neonatal jaundice with filtered sunlight in Nigerian neonates: study protocol of a non-inferiority, randomized controlled trial. Trials. 2013 Dec 28;14:446. doi: 10.1186/1745-6215-14-446.
Results Reference
derived

Learn more about this trial

Treatment of Neonatal Jaundice With Filtered Sunlight Phototherapy: Safety and Efficacy in African Neonates

We'll reach out to this number within 24 hrs