Thermal Imaging Compared to Skeletal Survey in Children Below 2 Years

Sponsor
Sheffield Children's NHS Foundation Trust (Other)
Overall Status
Completed
CT.gov ID
NCT04237454
Collaborator
(none)
2
1
1
7.3
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Study Details

Study Description

Brief Summary

When a child less than 2 years old attends the Emergency Department (ED) with an injury, carers should offer an explanation. When there is no explanation or if the explanation is inconsistent & because the child cannot say what happened, the doctor will need to consider all possible causes including child abuse. To help exclude abuse, the doctor will request x-rays of all the child's bones to make sure there are no other unexplained fractures. This requires up to 20 x-rays, which are called a skeletal survey. Even if there are no fractures, some or all of the x-rays will be repeated in the following 7-21 days, because by that time any fractures will have started to heal and so are easier to see than on the first skeletal survey. It means that if a doctor is worried about abuse, the child may need to have up to 40 x-rays, which amounts to a significant radiation dose (more than 6 months of natural UK background radiation) & increases the child's lifetime risk of getting cancer. 79 to 97 out of 100 skeletal surveys performed are normal. While it is of paramount importance to identify if a child is being abused, it is also important to minimise radiation dose. A camera which detects light and heat given off by the body has shown promise in some areas of medical practice. We plan to compare the results from the camera to those of the skeletal survey in 40 children below 2 years of age attending our hospital over a 6-month period. We hope to demonstrate that this technology can be used to further select children who should have a skeletal survey, reducing radiation dose in children without missing those who are being abused and sending them home to be abused again.

Condition or Disease Intervention/Treatment Phase
  • Device: Thermal Imaging Camera
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
2 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Thermal ImagingThermal Imaging
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Thermal Imaging Compared to Skeletal Survey for Diagnosis of Fractures in Suspected Inflicted Injury in Children Below 2 Years of Age: A Prospective Diagnostic Accuracy Study
Actual Study Start Date :
Sep 1, 2016
Actual Primary Completion Date :
Apr 11, 2017
Actual Study Completion Date :
Apr 11, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Infrared Imaging undertaken

Device: Thermal Imaging Camera
To develop a non-ionising radiation-based method of excluding fractures in children with suspected physical abuse

Outcome Measures

Primary Outcome Measures

  1. Diagnostic accuracy of thermal imaging for fracture detection compared to skeletal survey as the gold standard [6 months]

    Diagnostic accuracy (sensitivity, specificity, positive and negative predictive value) of thermal imaging compared to the full skeletal survey as gold standard

Secondary Outcome Measures

  1. Potential radiation dose reduction - calculated on the basis of known radiation exposure of the images that form the skeletal survey [6 months]

    Radiation dose saving of a protocol that only images those areas of abnormality seen on thermal imaging compared to the full skeletal survey as gold standard

  2. Carer acceptability/preference of the imaging modalities [6 months]

    Descriptive statistics based on responses to a non-validated questionnaire on carer experiences of both imaging techniques

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 16 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Children between 1 month and 2 years of age having initial/follow-up skeletal survey for investigation of suspected abuse

  • Healthy Control children

Exclusion Criteria:
    1. Informed consent withheld by main carer/guardian for the skeletal survey (court order would then be issues) 2. Informed consent for participation in the research study withheld 2. Situations where informed consent cannot be obtained (e.g. inability of carer/guardian to understand written English) 3. Postmortem cases (inclusion of the demised would unduly complicate the consent process for this small pilot study)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical Research Facility Sheffield South Yorkshire United Kingdom S10 2TH

Sponsors and Collaborators

  • Sheffield Children's NHS Foundation Trust

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sheffield Children's NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT04237454
Other Study ID Numbers:
  • SCH-13-067f
First Posted:
Jan 23, 2020
Last Update Posted:
Jan 23, 2020
Last Verified:
Jan 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 23, 2020