NCT07276334

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

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
13mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress25%
Jan 2026Jun 2027

First Submitted

Initial submission to the registry

November 29, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 11, 2025

Completed
21 days until next milestone

Study Start

First participant enrolled

January 1, 2026

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

January 15, 2026

Status Verified

January 1, 2026

Enrollment Period

12 months

First QC Date

November 29, 2025

Last Update Submit

January 14, 2026

Conditions

Distal Radius Fracture Fixation

Outcome Measures

Primary Outcomes (1)

  • Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire,

    A self-report tool (0-100) measuring upper limb function, where higher scores mean more disability,

    from surgery to one year after

Study Arms (2)

Same-day-discharge

EXPERIMENTAL
Procedure: early release from hospital

Hospitalized

ACTIVE COMPARATOR
Procedure: Day after surgery release

Interventions

early release from hospitalPROCEDURE

Same day discharge of patients undergoing distal radius operative fixation

Same-day-discharge
Day after surgery releasePROCEDURE

release of patients one day after surgery

Hospitalized

Eligibility Criteria

Age18 Years - 120 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients aged ≥18 years and
  • diagnosed with a DRF requiring surgical intervention and
  • booked for surgery

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shamir Medical Center

Ẕerifin, Israel, Israel

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

November 29, 2025

First Posted

December 11, 2025

Study Start

January 1, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

June 1, 2027

Last Updated

January 15, 2026

Record last verified: 2026-01

Locations

IL(1)