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Clinical Trials/NL-OMON38807
NL-OMON38807
Completed
Not Applicable

The effect of spinal anesthesia on pain perception and sedation in healthy volunteers - the SAPP study

eids Universitair Medisch Centrum0 sites16 target enrollmentTBD
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Conditions(chronische) neuropathische pijnchronic painneuropathic pain10034606

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
(chronische) neuropathische pijn
Sponsor
eids Universitair Medisch Centrum
Enrollment
16
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Healthy male volunteers, aged 18 to 45 years, right\-handed.

Exclusion Criteria

  • •\- Obesity (BMI \> 30\);
  • •\- Significant history of any cardiac or vascular disorder, asthma or other pulmonary disease, major gastrointestinal abnormalities, peptic ulceration, hepatic, neurological, psychiatric, hematological (including bleeding disorders), endocrine, renal, or major genitourinary disease;
  • •\- History of illness, condition or medication use that, in the opinion of the investigator, might interfere with optimal participation, confound the results of the study or pose additional risk in administering spinal anesthesia to the subject;
  • •\- History of chronic alcohol or illicit drug use;
  • •\- Metal medical devices like pacemakers, knee or hip prosthesis, ear implants, vessel clips, subcutaneous insulin pumps or carries metal particles (e.g. metal splinter in the eye) inside the body;
  • •\- Claustrophobia;
  • •\- Allergy to study medications;
  • •\- Not able to maintain a regular diurnal rhythm.

Outcomes

Primary Outcomes

Not specified

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