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The transition from acute to chronic pain in patients with acute musculoskeletal trauma

The transition from acute to chronic pain in patients with acute musculoskeletal trauma - PROTACT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38057
Enrollment
2200
Registered
2011-08-11
Start date
2011-09-19
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

acute en chronische pijn chronic pain musculoskeletal trauma

Interventions

None listed

Sponsors

Universiteit Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adult patients with injury to extremities of the musculoskeletal system, who are admitted to the emergency department of Medisch Spectrum Twente, The Netherlands. -injuries (fracture, soft tissue) due to a blunt trauma to the extremities of the musculoskeletal system -Age: 18 years till 69 years -Ability to read, speak and understand Dutch

Exclusion criteria

Exclusion criteria: - Patients with a life or limb threatening condition (i.e. Manchester Triage categories one or two, defines as patient who needs immediate treatment and should be seen by a physician within 10 minutes, with an exception for patients with luxations, fractures coded with MTS II, who did not have other trauma. These patients will receive a invitation after medical treatment) - Patients with polytrauma to the musculoskeletal system - Patients with cognitive disability

Design outcomes

Primary

MeasureTime frame
Main study endpoint is the development of chronic musculoskeletal pain. Primary outcomes are presence of pain (Yes/No) and pain severity (high/low intensity) at 3, 6, and 12 months follow-up. Information about potential risk factors (e.g. sociodemographics, pain -, injury and health characteristics) and health care utilization of each patient will be collected.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)