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

NCT ID: NCT07276334

Last Updated: 2025-12-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-01

Study Completion Date

2027-06-01

Brief Summary

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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

Detailed Description

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Conditions

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Distal Radius Fracture Fixation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Same-day-discharge

Group Type EXPERIMENTAL

early release from hospital

Intervention Type PROCEDURE

Same day discharge of patients undergoing distal radius operative fixation

Hospitalized

Group Type ACTIVE_COMPARATOR

Day after surgery release

Intervention Type PROCEDURE

release of patients one day after surgery

Interventions

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early release from hospital

Same day discharge of patients undergoing distal radius operative fixation

Intervention Type PROCEDURE

Day after surgery release

release of patients one day after surgery

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

120 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assaf-Harofeh Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Ofir Vinograd

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Ofir Vinograd, DR

Role: CONTACT

Phone: +972502260335

Email: [email protected]

Other Identifiers

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ASF-25-0106

Identifier Type: -

Identifier Source: org_study_id