Refraining from closed reduction of dislocated distal radius fractures in the emergency department

Refraining from closed reduction of dislocated distal radius fractures in the emergency department - RECORDED

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON53461

Enrollment

134

Registered

2023-01-27

Start date

2023-05-08

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

broken wrist upper extremity injury

Interventions

No reduction.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: patients aged 18-75 dislocated distal radius fracture requiring plate fixation

Exclusion criteria

Exclusion criteria: age 75 limb threatening injury (ischemia, compound fracture, nerve damage) multiple trauma patients previous injury imparing wrist function or previous fracture of ipsilateral wrist

Design outcomes

Primary

Measure	Time frame
The primary outcome is the average of the pre-operative Visual Analogue Scale for pain (VAS) score, reported on daily basis from the ED visit until operation.	—

Secondary

Measure	Time frame
Secondary outcomes are length of surgery, wrist function measured with the Patient Rated Wrist Evaluation (PRWE) score after six weeks and three, six and twelve months, length of stay in the ED, type and quantity of used pain medication, patient satisfaction and complications. Furthermore, a cost-effectiveness analysis will be performed.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)