Reproducibility of Results
Conditions
Keywords
Magnetic Resonance Imaging, Diffusion Tensor Imaging, Reproducibility of Results, Feasibility Study, Healthy Volunteers
Brief summary
The aim of this study is to assess the reproducibility over time of functional and structural magnetic resonance imaging, as well as specific biomarkers in plasma in healthy volunteers before and after a two-hour rest. This design mimics the timing of repeated scans and blood sampling before and after two hours of anaesthesia in subsequent substudies of the protocol, 'Neuroplasticity Induced by General Anaesthesia'.
Detailed description
In the study 'Neuroplasticity Induced by General Anaesthesia', the investigators intend to explore the effects of general anaesthesia on the brain by state-of-the-art magnetic resonance imaging (MRI). MRI data - especially changes in functional MRI recordings - may theoretically depend on a variety of physiological variables such as cerebral blood flow, cerebral blood volume, and cerebral metabolic oxidative rate of oxygen, and may thus also be affected by pharmacological agents. However, to interpret data it is important to know the inherent variability of the scans. This first substudy therefore aims to determine the reproducibility of the MRI recordings without administration of pharmacological agents. Another aim of the study is to ensure feasibility of the design before embarking on the more resource-demanding substudies in anaesthetised subjects. In this substudy, the investigators will perform the same MRI measurements as in the main study; rather than undergoing two hours of general anaesthesia, the volunteers will be subjected to two hours of undisturbed rest. Each participant goes through a pre-study interview and physical examination to ensure that the participant is healthy and suitable for participation. For each participant, the study consists of three study days: Day 0: Baseline MRI and blood tests. Intervention. Two hours of post-intervention care followed by post-intervention MRI and blood tests. Day +1 (the day after Day 0): MRI and blood tests. Day +7 (one week after Day 0): MRI and blood tests. All MRI scans will be performed with a 3 Tesla Philips Achieva d-stream with a 32-channel receive head coil. Blood tests: Haemoglobin, sodium, potassium, white blood count, C-reactive protein (CRP), S calcium-binding protein 100b (S100b), neuron-specific enolase (NSE), interleukin-1 (IL-1), IL-6, IL-8, IL-10, IL-18, tumor necrosis factor Alpha (TNF-Alpha) and transforming growth factor beta (TGF-beta).
Interventions
None listed
Sponsors
Rigshospitalet, Denmark
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes
Inclusion criteria
* Age ≥18 ≤35 * Healthy individual * Normal electrocardiogram (ECG) * Normal physical examination, including neurological examination, auscultation of the heart and lungs, and measurement of blood pressure and pulse. * Speaks and understands Danish * Provides oral and written informed consent * Right-handed * American Society of Anaesthesiologists (ASA) class 1 (2) * Mallampati I-II and simplified airway risk index (SARI) 0-2 (i.e. no indication of difficult intubation. See Appendix for details) * BMI ≥18 kg/m2 and ≤30kg/m2 * Female participants must use safe contraceptives.
Exclusion criteria
* Cannot cooperate to tests * Left-handedness or ambidexterity * History of cancer, immune disease, autoimmune disease, chronic pain, neurological / psychiatric illness or other serious illness * Pregnancy * Weakly intake of \>21 (males) or \>14 (females) units of alcohol * Substance abuse (assessed by the investigator) * Daily use of any medication (contraceptives allowed) * Consumed anti-depressants during the last 30 days before study days * Heavy intake of caffeine (\> 5 cups/day) * Smoking during the last 30 days before study days * Reflux or dyspepsia * Poor dental status or oral health * Contraindication to MRI * Allergy to any kind of medication or material to which the volunteer could be exposed to during this study * Family history of malignant hyperthermia * Declines receiving information regarding incidental pathological findings during MRI scans of the brain. * Otherwise judged unfit for participation by the investigator * Major trauma or head trauma with any symptoms present at the time of inclusion * Surgery less than six weeks prior to the study period * Infection (with fever) less than two weeks prior to the study period * Expected or suspected difficult airway * History of complications to general anaesthesia * Known incident of malignant hyperthermia or unexplained complications to general anaesthesia among close relatives.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Feasibility and reproducibility: rates of protocol violation and delays as well as adverse events | 8 days | Evaluation of feasibility of study set-up, as measured by rates of protocol violation and delays as well as adverse events. The time frame mentioned below runs from the first study day, NOT from eligibility interview. |
Countries
Denmark
Outcome results
None listed