VALIDATION STUDY: NOCICEPTIVE PAIN MODEL AND PHARMACOLOGICAL INTERVENTION

VALIDATION STUDY: NOCICEPTIVE PAIN MODEL AND PHARMACOLOGICAL INTERVENTION - NOCICEPTIVE PAIN MODEL VALIDATION STUDY

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON32823

Enrollment

Registered

2008-11-11

Start date

2008-12-08

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

acute pijn acute pain

Interventions

Ultiva (remifentanil) and inducing light pain sensations

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 18-40 years of age BMI 18-30

Exclusion criteria

Exclusion criteria: Evidence of clinically relevant pathology in the history

Design outcomes

Primary

Measure	Time frame
heat detection threshold (HDT), heat pain detection threshold (HPDT), heat pain, cold detection threshold (CDT), cold pain detection threshold (CPDT), cold pain, cold pressor pain, mechanical pain threshold (MPT) and pressure pain threshold (PPT) ; VAS pain intensity during heat pain, cold pain and cold pressor pain	—

Secondary

Measure	Time frame
AEs, oxygen saturation, heart rate and rhythm, blood pressure and respiratory rate	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)