CIVS

CPM inter-site variability study (CIVS)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON20823

Enrollment

Registered

2021-01-07

Start date

2021-01-11

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Healthy individuals

Interventions

Standard CPM protocol vs LUMC CPM protocol

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy according to medical history, physical examination and vital signs; 2. Age 18-40; 3. Able to give informed consent;

Exclusion criteria

Exclusion criteria: 1. Presence of health issues including clinical pain of any kind in the previous 3 months; 2. Any use of pain medication; 3. Pregnancy or lactation; 4. Participation in another study at the same time; 5. Presence of in dept knowledge or experience of/in CPM testing or CPM study methods 6. Presence of Raynaud phenomenon;

Design outcomes

Primary

Measure	Time frame
The main study outcome is the difference in CPM between the ‘standard’ protocol and the ‘home’ protocol.	—

Secondary

Measure	Time frame
Several questionnaires	—

Contacts

Public ContactCornelis Jan van Dam

Leiden University Medical Center

c.j.van_dam@lumc.nl071-5262301

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)