FENTANYL-INDUCED ANALGESIA AND EFFECT OF REVERSAL BY NALOXONE

FENTANYL-INDUCED ANALGESIA AND EFFECT OF REVERSAL BY NALOXONE - Fena study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON32414

Enrollment

Registered

2007-11-20

Start date

2007-12-01

Completion date

Unknown

Last updated

2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pijn nociception pain

Interventions

Infusion of opioid (fentanyl) and its antagonist (naloxone)

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy volunteers, aged 18-45 yrs

Exclusion criteria

Exclusion criteria: Obesity (BMI > 30); Presence of medical disease (heart-, lung-, liver-, kidney-, neurological disease; diabetes m.; pyrosis; diaphragmatic hernia); Presence of psychiatric disease; History of chronic alcohol or drug use; Allergy to study medications; Possibility of pregnancy; Lactation.

Design outcomes

Primary

Measure	Time frame
Pain relief using two pain assays (heat pain and electrical pain)	—

Secondary

Measure	Time frame
-	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)