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

Physiological and Psychosomatic Effects of Exposure to MRI Scanning Environment

Background:

- Magnetic resonance imaging (MRI) creates high-quality images of the human body without x-rays. It uses a strong magnetic field and radio waves to take pictures. Researchers want to test a scanner that uses a high magnetic field strength.

Objective:

- To study how the body responds to being in a high field 11.7T MRI scanner.

Eligibility:

- Healthy people ages 22 65.

Design:

  • Participants will be screened with a medical history and physical exam. They will complete a healthy volunteer questionnaire and an MRI safety screening form. They may have a 3T MRI scan of the brain.
  • Participants will have an MRI scan. They will lie on a table that will slide in and out of the MRI cylinder very slowly. They will be asked to lie still.
  • Participants will do simple tasks while inside the machine. These can include listening and responding to questions, tapping fingers, or moving a hand.
  • While in the scanner, participants will hear loud knocking noises. They will get earmuffs.
  • Right when they exit the scanner, participants will get a questionnaire to fill out. This will ask about how they felt inside the scanner.
  • During the MRI, participants heart rate, respiratory rate, and skin temperature will be measured. Before and after the scan, these things plus blood pressure will be measured.
  • Participants will be tested before and after being in the MRI scanner. They will answer questions, take pen-and-paper or computer tests, and do simple actions. Their sense of smell may be tested.

Studieöversikt

Status

Indragen

Betingelser

Detaljerad beskrivning

Objective

The goals of this pilot study are to establish a normative database of vital signs, cognitive function and unusual subjective sensations in a 0T scanner. This data will be used as a reference for a future study of the effects of exposure to a 11.7T static magnetic field.

Study Population

26 healthy volunteers, aged 22-65.

Accrual ceiling =50

Accrual Target =26

Drop outs will be replaced

Design

The study consists of one outpatient screening session and one experimental session. Informed consent and a history and neurological examination will be carried out at the screening visit. Vital signs (pulse oximeter, heart rate, respiratory rate and skin temperature) will be measured immediately before and after the experimental scan session, and pulse oximeter, heart rate and respiration will be monitored when the subject is in the scanner. Subjects will remain in the scanner for approximately 1 hour. During the experimental session, while the subject is in the scanner, they will be asked to carry out a brief test of attention at 10-15 minute intervals, up to 3 times during the session. At the end of the experimental session, subjects will fill out the MRI exit questionnaire to rate subjective sensations such as nausea, vertigo, and lightheadedness, on a Likert scale and complete a computerized neuro-cognitive test battery.

Outcome Measures

The objective of the study is to obtain a normative dataset of neuropsychological test measures, physiological parameters, and subjective experiences measures in subjects undergoing 0T exposure.

Studietyp

Observationell

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

22 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

  • INCLUSION CRITERIA:
  • 22 - 65 years of age
  • In good general health
  • Able to understand the procedures and requirements and give informed consent
  • Fluent in English

EXCLUSION CRITERIA:

All Subjects will answer the NMR safety screening form and the Healthy volunteer form A subject will be excluded if he/she:

  • Has any implanted medical device
  • Underwent brain surgery, have a central nervous system illness, a neurological lesion or history of neurological or psychiatric disorders
  • Medical problems, such as diabetes mellitus, hypertension, pulmonary or airway disease, heart failure, coronary artery disease, history of sleep apnea
  • Diagnosable substance dependence
  • Consumes more than 1 alcoholic drink per day for women and up to 2 drinks per day for men on a regular basis
  • Has any metal in their body due to by trauma or surgery
  • Cannot lie comfortably on their back for up to 60 minutes
  • Is pregnant
  • Have sustained shrapnel injuries
  • Has worked as a machinist, or other occupations that have resulted in metal shavings in their eye
  • Has claustrophobia
  • Has known hearing problems

Studieplan

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

Hur är studien utformad?

Designdetaljer

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
Neuropsychological tests
Tidsram: 2 years
2 years
Physiological parameters
Tidsram: 2 years
2 years
Subjective experience parameters
Tidsram: 2 years
2 years

Samarbetspartners och utredare

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

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

23 december 2014

Primärt slutförande (Faktisk)

27 september 2019

Avslutad studie (Faktisk)

27 september 2019

Studieregistreringsdatum

Först inskickad

15 januari 2015

Först inskickad som uppfyllde QC-kriterierna

15 januari 2015

Första postat (Uppskatta)

16 januari 2015

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

17 december 2019

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

14 december 2019

Senast verifierad

27 september 2019

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 150057
  • 15-N-0057

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