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SugarFACT - Sugar Requirements For African Children Trial

Primary Purpose

Hypoglycemia Non Diabetics, Emergencies, Pediatric ALL

Status
Terminated
Phase
Not Applicable
Locations
Malawi
Study Type
Interventional
Intervention
10% dextrose
Sponsored by
Helena Hildenwall
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypoglycemia Non Diabetics focused on measuring pediatric, critical illness, Malawi

Eligibility Criteria

1 Month - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age between one month to 5 years (5 to 12 years for outcome measure no 3)
  • Parent/carer willing and able to give consent
  • Presence of one or several emergency signs (as defined in WHO pocket book of hospital care for children)

    • Obstructed or absent breathing
    • Central cyanosis
    • Severe respiratory distress
    • Shock/impaired perfusion
    • Coma/reduced consciousness
    • Convulsions
    • Severe dehydration
  • Clinical concern that the child is in an emergency state
  • Blood glucose 2.5-5.0mmol/l at arrival to the emergency department (3.0-5.0mmol/l for severely malnourished children). For outcome measure no 4 children with <2.5 mmol/l on arrival who then have 2.5-5.0 mmol/l on the repeat test 30 minutes later are also included

Exclusion Criteria:

  • Children with a known diagnosis of diabetes
  • Refusal to participate by the child or guardians

Sites / Locations

  • Queen Elisabeth Central Hospital
  • Zomba Central Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Dextrose

Control

Arm Description

Children in the intervention group will immediately receive intravenous 5ml/kg 10% dextrose, Dextrose administration will continue as a maintenance infusion of intravenous 10% dextrose for 24 hours at standard maintenance rates. Capillary blood glucose monitoring will be repeated at 30 minute intervals with repeated equivalent bolus doses given until levels reach ≥5.0mmol/l. All children will be kept in the emergency department for a minimum of 60 minutes and have their vital signs checked at discharge from the emergency room to the ward.

Usual care - the care that is currently provided in the hospital - will be provided. All children in the control group will be kept in the emergency department for a minimum of 60 minutes and have their vital signs checked at discharge from the emergency room to the ward.

Outcomes

Primary Outcome Measures

In-hospital mortality in children 1 month to 5 years old
From date of randomization until the date of discharge from hospital or date of in-hospital death, whichever came first, assessed up to 12 months

Secondary Outcome Measures

24 hours mortality in children 1 month to 5 years old
Mortality within the first 24 hrs after admission

Full Information

First Posted
December 5, 2016
Last Updated
February 14, 2019
Sponsor
Helena Hildenwall
Collaborators
Kamuzu University of Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02989675
Brief Title
SugarFACT - Sugar Requirements For African Children Trial
Official Title
SugarFACT - Sugar Requirements For African Children Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Terminated
Study Start Date
December 2016 (undefined)
Primary Completion Date
January 22, 2019 (Actual)
Study Completion Date
January 22, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Helena Hildenwall
Collaborators
Kamuzu University of Health Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the impact of dextrose administration in severely sick children admitted to hospital with low-glycaemia. The problem: Mortality in children remains high in sub-Saharan African hospitals. While antimalarial drugs, antibiotics and other definitive treatments are well understood, the role of emergency care with supportive therapies such as maintaining normal glucose and electrolyte balances, has been given limited attention. Hypoglycaemia is common in children admitted to hospital in low-income settings. The current definition of hypoglycaemia is a blood glucose level of less than 2.5mmol/l. Outcomes for these children are poor, with a mortality rate of up to 42%. An increased mortality has also been reported among acutely ill children with low-glycaemia, defined as a blood glucose level of 2.5-5.0mmol/l. The reason for increased mortality rates is not fully understood. Study objective: To determine the impact on mortality of a raised treatment cut-off level for paediatric hypoglycaemia, from 2.5mmol/l to 5.0mmol/l. Methodology: Severely ill children admitted to two central Malawian hospitals; Queen Elisabeth Central Hospital, Blantyre and Zomba Central Hospital, with low-glycaemia (2.5-5.0mmol/l) will be randomised into intervention or control groups. The intervention group will be treated with an intravenous bolus of 10% dextrose 5ml/kg followed by a dextrose infusion in addition to standard care while the control group will receive standard care only. Children will be followed until discharge from hospital or death. Primary end-point is in-hospital mortality.
Detailed Description
Enrolment started at Queen Elisabeth Central Hospital on Dec 5th 2016. Due to a slow enrolment rate a second site at Zomba Central Hospital has been opened to start enrolment on October 17th, 2017 in order for the project to be completed in December 2019.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoglycemia Non Diabetics, Emergencies, Pediatric ALL, Critical Illness
Keywords
pediatric, critical illness, Malawi

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
410 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dextrose
Arm Type
Experimental
Arm Description
Children in the intervention group will immediately receive intravenous 5ml/kg 10% dextrose, Dextrose administration will continue as a maintenance infusion of intravenous 10% dextrose for 24 hours at standard maintenance rates. Capillary blood glucose monitoring will be repeated at 30 minute intervals with repeated equivalent bolus doses given until levels reach ≥5.0mmol/l. All children will be kept in the emergency department for a minimum of 60 minutes and have their vital signs checked at discharge from the emergency room to the ward.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Usual care - the care that is currently provided in the hospital - will be provided. All children in the control group will be kept in the emergency department for a minimum of 60 minutes and have their vital signs checked at discharge from the emergency room to the ward.
Intervention Type
Drug
Intervention Name(s)
10% dextrose
Intervention Description
Bolus of 10% dextrose 5mls/kg
Primary Outcome Measure Information:
Title
In-hospital mortality in children 1 month to 5 years old
Description
From date of randomization until the date of discharge from hospital or date of in-hospital death, whichever came first, assessed up to 12 months
Time Frame
Up to 12 months
Secondary Outcome Measure Information:
Title
24 hours mortality in children 1 month to 5 years old
Description
Mortality within the first 24 hrs after admission
Time Frame
24 hours after admission
Other Pre-specified Outcome Measures:
Title
In-hospital mortality in children 5-12 years old
Description
From date of randomization until the date of discharge from hospital or date of in-hospital death, whichever came first, assessed up to 12 months
Time Frame
Up to 12 months
Title
In hospital mortality in children with initial hypoglycaemia (blood glucose <2.5mmol/l) and low glycemia after first dextrose bolus
Description
From date of randomization until the date of discharge from hospital or date of in-hospital death, whichever came first, assessed up to 12 months
Time Frame
Up to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between one month to 5 years (5 to 12 years for outcome measure no 3) Parent/carer willing and able to give consent Presence of one or several emergency signs (as defined in WHO pocket book of hospital care for children) Obstructed or absent breathing Central cyanosis Severe respiratory distress Shock/impaired perfusion Coma/reduced consciousness Convulsions Severe dehydration Clinical concern that the child is in an emergency state Blood glucose 2.5-5.0mmol/l at arrival to the emergency department (3.0-5.0mmol/l for severely malnourished children). For outcome measure no 4 children with <2.5 mmol/l on arrival who then have 2.5-5.0 mmol/l on the repeat test 30 minutes later are also included Exclusion Criteria: Children with a known diagnosis of diabetes Refusal to participate by the child or guardians
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Helena Hildenwall, MD, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tim Baker, MD, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Queen Dube, MD, PhD
Organizational Affiliation
College of Medicine, Malawi
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Josephine Langton, MD
Organizational Affiliation
College of Medicine, Malawi
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Elisabeth Central Hospital
City
Blantyre
Country
Malawi
Facility Name
Zomba Central Hospital
City
Zomba
Country
Malawi

12. IPD Sharing Statement

Citations:
PubMed Identifier
33038950
Citation
Baker T, Ngwalangwa F, Masanjala H, Dube Q, Langton J, Marrone G, Hildenwall H. Effect on mortality of increasing the cutoff blood glucose concentration for initiating hypoglycaemia treatment in severely sick children aged 1 month to 5 years in Malawi (SugarFACT): a pragmatic, randomised controlled trial. Lancet Glob Health. 2020 Dec;8(12):e1546-e1554. doi: 10.1016/S2214-109X(20)30388-0. Epub 2020 Oct 8.
Results Reference
derived
PubMed Identifier
29325595
Citation
Baker T, Dube Q, Langton J, Hildenwall H. Mortality impact of an increased blood glucose cut-off level for hypoglycaemia treatment in severely sick children in Malawi (SugarFACT trial): study protocol for a randomised controlled trial. Trials. 2018 Jan 11;19(1):33. doi: 10.1186/s13063-017-2411-8.
Results Reference
derived

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SugarFACT - Sugar Requirements For African Children Trial

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