Skip to content

Prevalence of neuropathic pain in one year survivors after intensive care admission

Prevalence of neuropathic pain in one year survivors after intensive care admission - Neuropathic pain after critical illness

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45349
Enrollment
50
Registered
2017-03-08
Start date
2017-03-13
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Nerve pain

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Patient was 18 years or older at the time of ICU admission. 2. Length of stay in the ICU > 48 hours. 3. Recent address and vital (survivorship) status confirmed by follow-up survey. 4. Spoken informed consent from the patient is obtained during a telephone call Subsequent written informed consent from patient will be obtained during the home visit (before performing measurements).

Exclusion criteria

Exclusion criteria: Patients who are not competent to provide informed consent (i.e. patients with severe cognitive dysfunction).

Design outcomes

Primary

MeasureTime frame
The main study parameter is the prevalence of neuropathic pain in the study population as measured with the Douleur Neuropathique 4 (DN4) questionnaire. Besides 7 questions, this questionnaires contains also 3 items of short physical examination of the painful area.

Secondary

MeasureTime frame
Not applicable.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)