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The DICTION study

A description of the optimization of the ‘Overall Benefit of Analgesic Score’ and evaluation of usability and psychometric properties in clinical practice

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON21888
Enrollment
250
Registered
2021-04-19
Start date
2021-06-20
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

Postoperative pain

Interventions

None listed

Sponsors

Department of Anesthesiology, Amsterdam UMC, location AMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Aged eighteen years or older - Fluent in Dutch - Capable of completing the OBAS questionnaire - Has no objection to study inclusion - Underwent elective surgery that required overnight hospitalization - The performed surgery was orthopedic, trauma surgical, neurosurgical, abdominal or obstetric in nature

Exclusion criteria

Exclusion criteria: - ASA 5 or higher - Emergency surgery - Hospitalization at the intensive care unit (ICU), or previous admission to the ICU during the same hospital admission

Design outcomes

Primary

MeasureTime frame
The main study endpoint is the description of the psychometric properties of the optimized Dutch OBAS.

Secondary

MeasureTime frame
Secondary endpoints are determination of the MCID and clinical usability

Contacts

Public ContactPascal Smulders

Amsterdam UMC, location AMC

p.s.h.smulders@amsterdamumc.nl+31 20 566 2533

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)