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CompletedNCT03451669Infrared ShuntUpdated May 11, 2020

Thermal Camera Detection of Ventriculoperitoneal Shunt Flow

An observational study in Hydrocephalus, sponsored by University of Pennsylvania. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-05-11.

Sponsored by University of Pennsylvania · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2
Ages
18 Years and older
Sex
All
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Study summary

There have been reports in the past of using thermal cameras to demonstrate flow in the tubing as a surrogate of proper shunt function. This was shown to have almost 90% accuracy at determining proper functioning but required expensive equipment that was not universally available. There is now smart phone based thermal camera technology (Flir One: http://www.flir.com/flirone/) that could make this technique widely available for health care use. The goal of the study is to determine if this device can demonstrate flow in the distal tubing of a VP shunt.

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Conditions studied

  • Hydrocephalus

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03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Adult patients with VP shunts at the University of Pennsylvania, Department of Neurosurgery

Inclusion criteria

  • Patients with known VP shunt
  • Status of shunt function known.
  • Patients with well healed wounds (no immediately post op patients)

Exclusion criteria

Exclusion Criteria:

  • Patients in urgent need of shunt revision
  • Age less than 18
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2 participants (actual)
Patient registry
No

Groups and cohorts

  • Shunt suspected to be functioning
  • Shunt suspected to not be functioning
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What researchers measure

Primary outcomes

  1. Determine if a smartphone based thermal camera can determine flow in the distal tubing of a VP shunt.

    Time frame: 3 years

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Study locations

1 site
  • University of Pennsylvania Medical Center
    Philadelphia, Pennsylvania 19104, United States
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Registry details

Key details

Study ID
NCT03451669
Lead sponsor
University of Pennsylvania
Responsible party
Sponsor
First posted
Mar 2, 2018
Start date
Apr 16, 2018
Primary completion
Nov 30, 2019
Completion
Dec 2, 2019
Last update
May 11, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2020. You cannot join it, but the record below documents what was studied.

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