Pediatric Pneumonia Lung Ultrasound

NCT ID: NCT03187067

Last Updated: 2019-04-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

270 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-07-31

Study Completion Date

2019-01-08

Brief Summary

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The purpose of this study is to evaluate the impact of LUS on the diagnosis and management of childhood pneumonia in developing countries

Detailed Description

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Conditions

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Pneumonia Acute Respiratory Infection

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Mozambique, cases

Lung ultrasound

Intervention Type DEVICE

Lung ultrasound will be performed on all children to investigate imaging patterns characteristic of pneumonia.

Mozambique, controls

Lung ultrasound

Intervention Type DEVICE

Lung ultrasound will be performed on all children to investigate imaging patterns characteristic of pneumonia.

Pakistan, cases

Lung ultrasound

Intervention Type DEVICE

Lung ultrasound will be performed on all children to investigate imaging patterns characteristic of pneumonia.

Pakistan, controls

Lung ultrasound

Intervention Type DEVICE

Lung ultrasound will be performed on all children to investigate imaging patterns characteristic of pneumonia.

Interventions

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Lung ultrasound

Lung ultrasound will be performed on all children to investigate imaging patterns characteristic of pneumonia.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Male or female, 2 through 23 months of age
* Cough \<14 days or difficulty breathing
* Visible indrawing of the chest wall, with or without fast breathing
* Ability and willingness of child's caregiver to provide informed consent and to be available for follow-up for the planned duration of the study, including accepting a home visit if he/she fails to return to the study facility for a scheduled follow-up visit


* Male or female, 2 through 23 months of age
* Cough \<14 days or difficulty breathing
* Ability and willingness of child's caregiver to provide informed consent and to be available for follow-up for the planned duration of the study, including accepting a home visit if he/she fails to return to the study facility for a scheduled follow-up visit
Minimum Eligible Age

2 Months

Maximum Eligible Age

23 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bill and Melinda Gates Foundation

OTHER

Sponsor Role collaborator

Barcelona Institute for Global Health

OTHER

Sponsor Role collaborator

Aga Khan University

OTHER

Sponsor Role collaborator

Save the Children

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centro de Investigação em Saúde de Manhiça (CISM)

Manhiça, , Mozambique

Site Status

Aga Khan University

Karachi, , Pakistan

Site Status

Countries

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Mozambique Pakistan

References

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Riaz A, Cambaco O, Ellington LE, Lenahan JL, Munguambe K, Mehmood U, Lamorte A, Qaisar S, Baloch B, Kanth N, Nisar MI, Volpicelli G, Bassat Q, Jehan F, Ginsburg AS. Feasibility, usability and acceptability of paediatric lung ultrasound among healthcare providers and caregivers for the diagnosis of childhood pneumonia in resource-constrained settings: a qualitative study. BMJ Open. 2021 Mar 11;11(3):e042547. doi: 10.1136/bmjopen-2020-042547.

Reference Type DERIVED
PMID: 33707268 (View on PubMed)

Lenahan JL, Volpicelli G, Lamorte A, Jehan F, Bassat Q, Ginsburg AS. Multicentre pilot study evaluation of lung ultrasound for the management of paediatric pneumonia in low-resource settings: a study protocol. BMJ Open Respir Res. 2018 Dec 19;5(1):e000340. doi: 10.1136/bmjresp-2018-000340. eCollection 2018.

Reference Type DERIVED
PMID: 30622716 (View on PubMed)

Other Identifiers

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PLUS

Identifier Type: -

Identifier Source: org_study_id

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