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OpenTrials
Completed

NCT Number: NCT03451669

Thermal Camera Detection of Ventriculoperitoneal Shunt Flow

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Pennsylvania Medical Center

Philadelphia, Pennsylvania, 19104, United States

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

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

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Registry information

Acronym: Infrared Shunt

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 2, 2018
Registry last updated
May 11, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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