Contribution of norketamine to ketamine-induced antinociception,and cardiovascular and neurocognitive effects - NorKet

• Conditions: Pain induced in healthy volunteers; MedDRA version: 9.1Level: LLTClassification code 10066714Term: Acute pain

• Registration Number: EUCTR2008-002638-31-NL
• Lead Sponsor: MC

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2008-05-29
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: Male
• Target Recruitment: Not specified

Inclusion Criteria

Healthy male volunteers in the age of 18-45 years
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Obesity (BMI > 30);
Presence of medical disease (heart-, lung-, liver-,
kidney-, neurologic disease; diabetes m.; pyrosis;
diaphragmatic hernia);
Presence of psychiatric disease;
History of chronic alcohol or illicit drug use;
Allergy to study medications;
Color blindness;
Use of contact lenses.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified