Same Day Discharge Vs. Hospitalization for Operative Fixation of Distal Radius Fractures

NCT07276334 · tracked via the Priya Life Science Israel tracker

Sponsor

Assaf-Harofeh Medical Center

Phase

Not applicable

Started

2026-01-01

Last updated

2026-01-15

Condition(s) studied

Distal Radius Fracture Fixation

Investigational drug(s) / intervention(s)

early release from hospitalDay after surgery release

early release from hospital: Same day discharge of patients undergoing distal radius operative fixation

Day after surgery release: release of patients one day after surgery

Study 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

Eligibility

Sex

ALL

Min age

18 Years

Max age

120 Years

Healthy volunteers

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

Primary outcome measure(s)

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,

Trial sites (1)

Facility	City	Region	Status
Shamir Medical Center	Ẕerifin	Israel

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07276334 on ClinicalTrials.gov ↗ ← All trials in Israel