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Pain management after conservative treatment of extremity fractures, a randomized clinical trial

Pain management after conservative treatment of extremity fractures, a randomized clinical trial - Pain management after extremity fractures (conservative)

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39558
Enrollment
60
Registered
2012-05-14
Start date
Unknown
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

pijn broken bones Pain after fractures

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All adult patients (age > 18) who will receive conservative treatment for an extremity fracture.

Exclusion criteria

Exclusion criteria: Pregnant, breastfeeding or possibly pregnant patients and patients with relevant drug allergies will be excluded from study participation Further exclusion criteria include: 1) phalangeal fractures; 2) stress fractures; 3) another fracture at any site; 4) pathological fractures; 5) inability to fill out questionnaires; 6) polytrauma patients with other significant injuries outside the skeletal system; 7) patients already receiving any chronic form of analgesic prior to injury; 8) liver or renal dysfunction; 9) diagnosed constipation; 10) patients receiving MAO-inhibitors.

Design outcomes

Primary

MeasureTime frame
The main study parameters are the outcomes of the pain/satisfaction Numeric Rating Scale.

Secondary

MeasureTime frame
The secondary study parameters are the outcomes of the self-efficacy scale and the disability questionnaire.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)