Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Infrared Imaging in Septic Illness

10 februari 2020 uppdaterad av: University Hospitals, Leicester

The Application of Infrared Thermal Imaging in the Diagnosis and Prognostication of Septic Illness in Adults

The application of infrared thermal imaging in the diagnosis and prognostication of septic illness in adults.

During times of severe infection (sepsis), the small blood vessels supplying oxygen and nutrients to the skin and other organs (called the microcirculation), become abnormal and do not function as they normally would in health. Monitoring these small blood vessels is difficult to do clinically and the investigators want to investigate a new way of doing this.

The aim of this study is to validate a novel method of assessing the function of the microcirculation in healthy volunteers and patients with sepsis, by measuring the skin temperature profile of the leg and face with a thermal imaging camera. Thermal imaging cameras measure the heat given off by all objects and represents this as a picture, with colour used to represent the different temperatures.

Patients will be recruited from the Emergency Department and Intensive Care Units at University Hospitals of Leicester in to one of two groups based on their illness severity; uncomplicated sepsis and severe sepsis. Healthy volunteers will be recruited in to a third group. Recruitment will take place over a 6-month period with follow-up lasting for 12-months following recruitment. 105 participants will be recruited in total.

Temperature patterns seen on the face and leg will be investigated between the different groups. Changes in these temperature patterns as patients recover from sepsis (or indeed become worse), will also be investigated. Information from the thermal images will be correlated to routinely measured markers of infection, including clinical measurements (blood pressure, pulse, etc) and routine blood investigations.

Studieöversikt

Status

Avslutad

Betingelser

Intervention / Behandling

Studietyp

Observationell

Inskrivning (Faktisk)

112

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Leicestershire
      • Leicester, Leicestershire, Storbritannien, LE1 5WW
        • University Hospitals of Leicester

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

This study will involve the recruitment of acutely unwell patients from the Emergency Department and Intensive Care Unit areas of the hospital, alongside healthy volunteers.

Beskrivning

Inclusion Criteria:

  1. Male or Female, aged 18 years or above.
  2. Healthy volunteers - free from acute illness; will include staff and students at the University of Leicester and UHL, and patient relatives.
  3. Patient with septic illness will be recruited in to one of two groups depending on their disease severity - Sepsis (without evidence of organ dysfunction) or severe sepsis (with organ dysfunction).
  4. Able (in the Investigators opinion) and willing to comply with all study requirements.

Exclusion Criteria:

  1. Patient refusal
  2. Inability to gain appropriate assent/consent
  3. Children
  4. Prisoners or in police custody
  5. Skin marking likely to preclude image analysis (such as extensive tattoos).

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Observationsmodeller: Kohort
  • Tidsperspektiv: Blivande

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Friska volontärer
Patients in all groups will undergo infrared thermal imaging of the face and anterior leg (centered on the knee)
Sepsis
Patients in all groups will undergo infrared thermal imaging of the face and anterior leg (centered on the knee)
Severe sepsis/septic shock
Patients in all groups will undergo infrared thermal imaging of the face and anterior leg (centered on the knee)

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Measure the extent of thermally apparent mottling of the anterior knee using a previously described mottling score.
Tidsram: 18 months
Measure the extent of mottling (graded from 1 to 5) using the mottling score described by Ait-Oufella et al.
18 months
Measure core-peripheral temperature difference by means of a facial thermal image (Thermal Core-Peripheral Temperature Difference - TCPTD).
Tidsram: 18 months
Thermal core-peripheral temperature difference (TCPTD) will be assessed using temperature at the medial canthus (core) and nasal (peripheral) in degrees centigrade.
18 months

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Association between the severity of thermally derived mottling score and the Sequential Organ Failure Assessment (SOFA) score.
Tidsram: 18 months
Association between mottling score (graded 1-5) and illness severity as determined by the SOFA score (0-24).
18 months
Association between the severity of thermally derived mottling score and the APACHE II score.
Tidsram: 18 months
Association between mottling score (1-5) and illness severity as determined by the APACHE II score (0-71).
18 months
Association between the extent of Thermal Core Peripheral Temperature Difference (TCPTD) and the SOFA score.
Tidsram: 18 months
Associations between TCPTD (degrees centigrade) and illness severity as determined by the SOFA score (0-24).
18 months
Association between the extent of Thermal Core Peripheral Temperature Difference (TCPTD) and the APACHE II score.
Tidsram: 18 months
Associations between TCPTD (degrees centigrade) and illness severity as determined by the APACHE II score (0-71).
18 months
Mortality at 30 days and 1 year from the point of enrollment.
Tidsram: 18 months
Mortality information will be collected at 30 days and 1 year from the point of patient enrollment (0-6 months) and correlated to the thermally derived mottling score and thermal core-peripheral temperature difference to assess for potential prognostic value of the above investigations.
18 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Jonathan Thompson, MB ChB, BSc, MD, University Hospitals, Leicester

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 juli 2016

Primärt slutförande (Faktisk)

1 februari 2019

Avslutad studie (Faktisk)

1 februari 2019

Studieregistreringsdatum

Först inskickad

20 juni 2016

Först inskickad som uppfyllde QC-kriterierna

3 augusti 2016

Första postat (Uppskatta)

4 augusti 2016

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

11 februari 2020

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

10 februari 2020

Senast verifierad

1 februari 2020

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • UHL 11486

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

produkt tillverkad i och exporterad från U.S.A.

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera