Same Day Discharge Vs. Hospitalization for Operative Fixation of Distal Radius Fractures
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: early release from hospital, Day after surgery release.
- Who it may be relevant to
- Registry conditions: Distal Radius Fracture Fixation. Basic parameters: 18 years — 120 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Israel
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Outpatient vs. Inpatient Surgery for Distal Radius Fractures: A Prospective Randomized Trial
Overview
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
- Procedure early release from hospital
Same day discharge of patients undergoing distal radius operative fixation - Procedure Day after surgery release
release of patients one day after surgery
Primary outcome measures
- Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire, [Time frame: from surgery to one year after]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Israel · 1 center
- Shamir Medical Center — Ẕerifin
Identifiers
NCT: NCT07276334 · ASF-25-0106