Distal Radius Fracture Fixation
Conditions
Brief summary
The goal of this clinical trial is to examine the results for same-day discharge after distal radius operative fixation in adult pupolation. The main questions it aims to answer are: Is same day discharge safe and effective for distal radius fractures? Are the functional and patient reported outcome measures results different between same day discharge and hospitalized patients? Researchers will compare same day discharge patients with jospitalized patients to see if there are any differences between the groups Participants will: * undergo surgery * atend outpatient clinical follow up visits * answer dedicated questioneres
Interventions
PROCEDUREearly release from hospital
Same day discharge of patients undergoing distal radius operative fixation
PROCEDUREDay after surgery release
release of patients one day after surgery
Sponsors
Assaf-Harofeh Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
No
Inclusion criteria
* Patients aged ≥18 years and * diagnosed with a DRF requiring surgical intervention and * booked for surgery
Exclusion criteria
* Refusal to participate in the study * lack of follow-up * incomplete clinical or radiologic documentation * significant cardiac or pulmonary comorbidities * inadequate social support at home
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire, | from surgery to one year after | A self-report tool (0-100) measuring upper limb function, where higher scores mean more disability, |
Countries
Israel
Outcome results
None listed