DRKS00000663
Completed
Phase 4
Investigation of nociceptive and antinociceptivemechanisms under anesthesia using fMRI, EEG and noxious reflexes - fMRT-Nociception
Charité Campus Charité Mitte0 sites13 target enrollmentDecember 17, 2012
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- ociception under anesthesia in healthy participants
- Sponsor
- Charité Campus Charité Mitte
- Enrollment
- 13
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •informed consent; age 18\-60; no enrollment in other studies under the AMG (German medicinal products law)
Exclusion Criteria
- •any light or severe illness, especially even at the lightest stage: infections of the respiatory system, muscular diseases, diseases of the cns, chronical pain diseases, drug abuse, medication abuse; claustrophobia; increased risk of aspiration, especially adipositas (BMI \> 30 kg/m2\); pregnancy and lactation; history or family history of malign hyperthermia; history of family history of severe allergic reactions to propofol, remifentanil, soja, latex; placement in an institution on official order; implants, especially: pace makers, implanted cardioverters, cochlea implants, insulin pumps, nerve stimulators, vascular clips, cava filters, metal splints, screws, wires, plates; extensive or looped tattoos, unremovable piercings, other ferro\-magnetic body onaments; unwillingness to comply to the filing and transmission of pseudonymous data about diseases in the scope of the clinical trial; actual of expected future dependence of the study personnell
Outcomes
Primary Outcomes
Not specified
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