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CPM inter-site variability study (CIVS)

CPM inter-site variability study (CIVS) - CIVS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON49156
Enrollment
40
Registered
2020-12-24
Start date
2021-01-11
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

geen aandoening, onderzoek naar endogene pijnstilling endogenous pain modulation

Interventions

CPM tests - a method to quantify endogenous pain modulation

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Healthy according to medical history, physical examination and vital signs; -Age 18-40; -Able to give informed consent;

Exclusion criteria

Exclusion criteria: -Presence of health issues including clinical pain of any kind in the previous 3 months; -Use of continuous pain medication; -Pregnancy or lactation; -Participation in another study at the same time; -Presence of in dept knowledge or experience of/in CPM testing or CPM study methods

Design outcomes

Primary

MeasureTime frame
Explore the factors that contribute to CPM variability in order to optimize testing protocols and minimize variability

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)