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Solar Oxygen Study (SOS)

Primary Purpose

Pneumonia, Hypoxemia

Status
Completed
Phase
Not Applicable
Locations
Uganda
Study Type
Interventional
Intervention
Solar-powered oxygen
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pneumonia focused on measuring solar, oxygen

Eligibility Criteria

1 Month - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age under 5 years
  2. Hypoxemia (SpO2<92%) based on non-invasive pulse oximetry
  3. Hospital admission warranted based on clinician judgment

Exclusion Criteria:

  1. SpO2 ≥92%
  2. Outpatient management
  3. Denial of consent to participate in study

Sites / Locations

  • Adumi Health Centre IV
  • Apac District Hospital
  • Atiak Health Centre IV
  • Bugobero Health Centre IV
  • Bukedea Health Centre IV
  • Bumanya Health Centre IV
  • Bundibugyo Hospital
  • Kagadi Hospital
  • Kalisizo Hospital
  • Kamuli General Hospital
  • Kayunga District Hospital
  • Kidera Health Centre IV
  • Kitagata Hospital
  • Kitgum General Hospital
  • Kyenjojo General Hospital
  • Lalogi Health Centre IV
  • Lyantonde Hospital
  • Gombe Hospital
  • Muyembe Health Centre IV
  • Sembabule Health Centre IV

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Solar-powered oxygen

Standard of care

Arm Description

Solar panels used to drive an oxygen concentrator will deliver medical grade oxygen at a rate of 1-5L/min, for the treatment of children with hypoxemia.

Patients presenting with hypoxemia and pneumonia will be treated by standard of care prior to the implementation of solar-powered oxygen at a chosen site. This may include some allocation of oxygen via cylinders, but will likely be minimal or not available.

Outcomes

Primary Outcome Measures

Mortality
Mortality at 48 hours after admission

Secondary Outcome Measures

In hospital mortality
Mortality during any point of hospital admission
Length of hospital stay
Total length of hospital admission
Oxygen saturation
Measured oxygen saturations before and after administration of oxygen, using standard procedures
Oxygen delivery system failure
Number and duration of failures in any component of the oxygen delivery system, including solar panels, batteries, oxygen concentrator, and electrical components
Total costs of implementing solar-powered oxygen delivery systems
Total costs of implementing solar-powered oxygen delivery systems at twenty sites, including installation, servicing and maintenance

Full Information

First Posted
February 21, 2019
Last Updated
February 15, 2022
Sponsor
University of Alberta
Collaborators
Global Health Uganda LTD
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1. Study Identification

Unique Protocol Identification Number
NCT03851783
Brief Title
Solar Oxygen Study
Acronym
SOS
Official Title
Effect of Solar Powered Oxygen Delivery on Childhood Mortality in Uganda: A Cluster-Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
December 17, 2021 (Actual)
Study Completion Date
December 20, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alberta
Collaborators
Global Health Uganda LTD

4. Oversight

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

5. Study Description

Brief Summary
Globally, approximately 7.7 million children per year die before the age of 5 years. Infectious diseases account for a large proportion of these deaths, with pneumonia being the leading cause of mortality (2.1 million deaths/year). Most deaths occur in resource-poor settings in Asia and Africa. Oxygen (O2) therapy is essential to support life in these patients. Large gaps remain in the case management of children presenting to African hospitals with respiratory distress, including essential supportive therapies such as supplemental oxygen. In resource-constrained settings, oxygen delivery systems can lead to measurable improvements in survival from childhood pneumonia. A multihospital effectiveness study in Papua New Guinea demonstrated a reduction in mortality from childhood pneumonia from 5.0% to 3.2% (35% reduction in mortality) after implementation of enhanced oxygen delivery system. The investigators propose to investigate a novel strategy for oxygen delivery that could be implemented in remote locations with minimal access to an electrical power supply: solar-powered oxygen (SPO2).
Detailed Description
Clinical features of pneumonia in children include fever, respiratory distress, and hypoxemia. Respiratory distress is a useful clinical summary description with good inter-observer consistency among experienced medical practitioners. The following clinical signs may indicate increased work of breathing: sustained nasal flaring; indrawing (recession) of the bony structures of the chest wall (subcostal, intercostal, supraclavicular) on inspiration; tracheal tug; and deep breathing (acidotic or Kussmaul breathing). Respiratory distress is a sign that one or more serious pathological processes are at play: metabolic acidosis, fluid overload, acute lung injury, and/or co-morbid pneumonitis. Respiratory distress, together with alteration of consciousness, is a strong predictor of mortality in children with severe febrile illness in sub-Saharan Africa. The grim prognostic significance of respiratory distress applies to several disease states, irrespective of microbial etiology, including malaria as well as non-malaria febrile illness. Arterial hypoxemia in pneumonia results from several mechanisms: pulmonary arterial blood flow to consolidated lung resulting in an intrapulmonary shunt, intrapulmonary oxygen consumption, and ventilation-perfusion mismatch. Hypoxemia is a risk factor for mortality in pediatric pneumonia, and was associated with a 5-fold increased risk of death in studies from Kenya and Gambia. In one report from Nepal, the prevalence of hypoxemia (SpO2 < 90%) in 150 children with pneumonia was 39% overall, with increasing rates of hypoxemia across strata of pneumonia severity (100% of very severe, 80% of severe and 17% of pneumonia patients). General features of respiratory distress were associated with hypoxemia in this study, including chest indrawing, lethargy, grunting, nasal flaring, cyanosis, inability to breastfeed or drink. Oxygen is a lifesaving therapy for children with pneumonia and hypoxemia; however, challenges remain in oxygen delivery globally. Two main systems of oxygen delivery have been implemented and evaluated in resource-constrained settings, oxygen cylinders and oxygen concentrators. Oxygen cylinders are ready to use, simple to operate and do not require any electricity. However, cylinders are very costly and distribution and use is challenging. Oxygen concentrators have proven to be an effective means of delivering oxygen and are significantly less expensive that cylinders. However, oxygen concentrators require continuous and reliable electricity to operate which is not readily available in many regions, particularly in resource-limited settings where the majority of pneumonia deaths occur. In order to meet the demand for oxygen therapy in resource-limited settings, the investigators developed a novel strategy for oxygen delivery: solar-powered oxygen (SPO2). This system uses free inputs (sun and air) and could be implemented in remote locations with minimal access to an electrical power supply. Our group is the first to conduct rigorous scientific trials of SPO2. To date, the investigators have accumulated substantial clinical experience with SPO2, having treated >150 hypoxemic children, over several years, at two Ugandan hospitals. Compared to other oxygen delivery methods, SPO2 is superior. SPO2 is more reliable than oxygen concentrators connected to grid electricity, because it is not affected by frequent power outages. SPO2 utilizes a renewable, sustainable and freely available source of energy. SPO2 is more reliable than compressed oxygen cylinders, which are frequently out of stock in the public hospital system. SPO2 is more user-friendly and safer for nurses than cylinders, which require physical strength to change regulators on high-pressure cylinders. SPO2 is less wasteful than cylinders, which tend to leak through ill-fitting regulators under real-world conditions. The study is a multi-centre prospective evaluation of SPO2. The investigators will use a stepped-wedge cluster-randomized design to allow for robust scientific conclusions about the efficacy of SPO2. Importantly, demonstration of a mortality benefit of SPO2 will provide strong supportive evidence and could catalyse the widespread implementation of SPO2 in resource-limited settings across Africa and Asia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pneumonia, Hypoxemia
Keywords
solar, oxygen

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Stepped-wedge cluster randomized controlled trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2405 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Solar-powered oxygen
Arm Type
Experimental
Arm Description
Solar panels used to drive an oxygen concentrator will deliver medical grade oxygen at a rate of 1-5L/min, for the treatment of children with hypoxemia.
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Patients presenting with hypoxemia and pneumonia will be treated by standard of care prior to the implementation of solar-powered oxygen at a chosen site. This may include some allocation of oxygen via cylinders, but will likely be minimal or not available.
Intervention Type
Device
Intervention Name(s)
Solar-powered oxygen
Intervention Description
Constant and reliable administration of oxygen, using solar panels to power an oxygen concentrator and deliver medical grade oxygen at 1-5L/min.
Primary Outcome Measure Information:
Title
Mortality
Description
Mortality at 48 hours after admission
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
In hospital mortality
Description
Mortality during any point of hospital admission
Time Frame
Until end of hospitalization (usually 3 to 7 days)
Title
Length of hospital stay
Description
Total length of hospital admission
Time Frame
Until end of hospitalization (usually 3 to 7 days)
Title
Oxygen saturation
Description
Measured oxygen saturations before and after administration of oxygen, using standard procedures
Time Frame
Until end of hospitalization (usually 3 to 7 days)
Title
Oxygen delivery system failure
Description
Number and duration of failures in any component of the oxygen delivery system, including solar panels, batteries, oxygen concentrator, and electrical components
Time Frame
Until end of trial (24 months)
Title
Total costs of implementing solar-powered oxygen delivery systems
Description
Total costs of implementing solar-powered oxygen delivery systems at twenty sites, including installation, servicing and maintenance
Time Frame
Until end of trial (24 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Month
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age under 5 years Hypoxemia (SpO2<92%) based on non-invasive pulse oximetry Hospital admission warranted based on clinician judgment Exclusion Criteria: SpO2 ≥92% Outpatient management Denial of consent to participate in study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael T Hawkes, MD, PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Robert O Opoka, MBChB, MPH
Organizational Affiliation
Makerere University/Global Health Uganda
Official's Role
Principal Investigator
Facility Information:
Facility Name
Adumi Health Centre IV
City
Adumi
Country
Uganda
Facility Name
Apac District Hospital
City
Apac
Country
Uganda
Facility Name
Atiak Health Centre IV
City
Atiak
Country
Uganda
Facility Name
Bugobero Health Centre IV
City
Bugobero
Country
Uganda
Facility Name
Bukedea Health Centre IV
City
Bukedea
Country
Uganda
Facility Name
Bumanya Health Centre IV
City
Bumanya
Country
Uganda
Facility Name
Bundibugyo Hospital
City
Bundibugyo
Country
Uganda
Facility Name
Kagadi Hospital
City
Kagadi
Country
Uganda
Facility Name
Kalisizo Hospital
City
Kalisizo
Country
Uganda
Facility Name
Kamuli General Hospital
City
Kamuli
Country
Uganda
Facility Name
Kayunga District Hospital
City
Kayunga
Country
Uganda
Facility Name
Kidera Health Centre IV
City
Kidera
Country
Uganda
Facility Name
Kitagata Hospital
City
Kitagata
Country
Uganda
Facility Name
Kitgum General Hospital
City
Kitgum
Country
Uganda
Facility Name
Kyenjojo General Hospital
City
Kyenjojo
Country
Uganda
Facility Name
Lalogi Health Centre IV
City
Lalogi
Country
Uganda
Facility Name
Lyantonde Hospital
City
Lyantonde
Country
Uganda
Facility Name
Gombe Hospital
City
Mpigi
Country
Uganda
Facility Name
Muyembe Health Centre IV
City
Muyembe
Country
Uganda
Facility Name
Sembabule Health Centre IV
City
Sembabule
Country
Uganda

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27084827
Citation
Turnbull H, Conroy A, Opoka RO, Namasopo S, Kain KC, Hawkes M. Solar-powered oxygen delivery: proof of concept. Int J Tuberc Lung Dis. 2016 May;20(5):696-703. doi: 10.5588/ijtld.15.0796.
Results Reference
background
PubMed Identifier
29800014
Citation
Hawkes MT, Conroy AL, Namasopo S, Bhargava R, Kain KC, Mian Q, Opoka RO. Solar-Powered Oxygen Delivery in Low-Resource Settings: A Randomized Clinical Noninferiority Trial. JAMA Pediatr. 2018 Jul 1;172(7):694-696. doi: 10.1001/jamapediatrics.2018.0228.
Results Reference
background
PubMed Identifier
31805985
Citation
Conradi N, Mian Q, Namasopo S, Conroy AL, Hermann LL, Olaro C, Amone J, Opoka RO, Hawkes MT. Solar-powered oxygen delivery for the treatment of children with hypoxemia: protocol for a cluster-randomized stepped-wedge controlled trial in Uganda. Trials. 2019 Dec 5;20(1):679. doi: 10.1186/s13063-019-3752-2.
Results Reference
derived

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Solar Oxygen Study

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