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Clinical Trials/DRKS00000663
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.

Registry
who.int
Start Date
December 17, 2012
End Date
August 19, 2013
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Charité Campus Charité Mitte

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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