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Unipolar Versus Bipolar Interlocking in Humeral Shaft Fractures in Adults (UNILOCH)

Primary Purpose

Humeral Shaft Fracture

Status
Recruiting
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
questionnaires
scanner
Sponsored by
Centre Hospitalier Universitaire Dijon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Humeral Shaft Fracture

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patient with written consent Patient ≥18 years of age with a diagnosis of humeral shaft fracture (all types in the AO classification) requiring surgical treatment with intramedullary nailing Exclusion Criteria: Person not affiliated to national health insurance Patient unable to attend all study visits Patient with a pathologic fracture Patient with a post-traumatic brachial plexus injury at the time of inclusion Patient under court protection, guardianship or legal guardianship Pregnant, parturient or breastfeeding woman Patient admitted for revision surgery of a humerus fracture (insufficient healing or complication) Patient with an acute or chronic, unstable or poorly controlled disease that may interfere with the evaluation of the study objective, as determined by the investigator.

Sites / Locations

  • Chu Dijon BourgogneRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Unipolar interlocking group

Bipolar interlocking group

Arm Description

Outcomes

Primary Outcome Measures

The proportion of patients with radiologically assessed bone healing at 12 months

Secondary Outcome Measures

Full Information

First Posted
May 17, 2023
Last Updated
July 10, 2023
Sponsor
Centre Hospitalier Universitaire Dijon
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1. Study Identification

Unique Protocol Identification Number
NCT05877014
Brief Title
Unipolar Versus Bipolar Interlocking in Humeral Shaft Fractures in Adults
Acronym
UNILOCH
Official Title
Unipolar Versus Bipolar Interlocking in Humeral Shaft Fractures in Adults
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 3, 2023 (Actual)
Primary Completion Date
September 2027 (Anticipated)
Study Completion Date
September 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire Dijon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Shaft fractures account for 20% of humeral fractures and 3% of all adult fractures in France, with an estimated incidence of 13 to 20/100,000 people. Men aged 21 to 30 years and women aged 60 to 80 years are particularly affected. Intramedullary nailing is among the standard treatments for humeral shaft fractures (when surgery is required). Once inserted, the nail is locked in order to limit stress on the fractured bone, as well as possible secondary rotational displacements or malunion. Bipolar interlocking (BI) is typically performed on both sides (proximal and distal) of the fracture site. This procedure is performed under radiological control, exposing the patient and care team to radiation (during the entire procedure). The objective of the treatment is to obtain consolidation of the fracture within 12 months, and to limit the occurrence of irreversible complications such as malunion or nonunion (2-10% at 12 months post-surgery). The "unipolar interlocking" (UI) technique has recently been introduced. In this technique, locking is performed only on the proximal side of the fracture site. By avoiding the distal approach, potential complications such as radial nerve damage, with the risk of irreversible paralysis (3.8-14.2% in studies of the BI technique in this indication) or the risk of infection on the distal side can be avoided. It also reduces operative time, and consequently the radiation received by patients and caregivers. However, the UI may be poorly positioned, resulting in malunion that requires revision surgery. Despite the absence of recommendations due to the lack of existing data, several teams use the UI in routine care. In this context, a descriptive cohort of 121 patients operated on at the Dijon University Hospital5 showed similar rates of consolidation between the 2 techniques (93.8% for UI versus 95.2% for BI, p=0.64), functional scores, and complications, as well as a significant 29% decrease in operating time in the UI group (mean + SD: 63.1±21.3 min versus 88.0±30.1 min for VB, p<0.01). These encouraging results, although limited by the retrospective and observational nature of the data, justify a prospective randomized trial comparing these two techniques.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Humeral Shaft Fracture

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
390 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Unipolar interlocking group
Arm Type
Experimental
Arm Title
Bipolar interlocking group
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
questionnaires
Intervention Description
EQ-5D-5L and SF-12
Intervention Type
Other
Intervention Name(s)
scanner
Intervention Description
CT scan at M9 and then at M12 if the humerus is not consolidated at M6
Primary Outcome Measure Information:
Title
The proportion of patients with radiologically assessed bone healing at 12 months
Time Frame
Through study completion, an average of 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient with written consent Patient ≥18 years of age with a diagnosis of humeral shaft fracture (all types in the AO classification) requiring surgical treatment with intramedullary nailing Exclusion Criteria: Person not affiliated to national health insurance Patient unable to attend all study visits Patient with a pathologic fracture Patient with a post-traumatic brachial plexus injury at the time of inclusion Patient under court protection, guardianship or legal guardianship Pregnant, parturient or breastfeeding woman Patient admitted for revision surgery of a humerus fracture (insufficient healing or complication) Patient with an acute or chronic, unstable or poorly controlled disease that may interfere with the evaluation of the study objective, as determined by the investigator.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pierre MARTZ
Phone
0380293307
Ext
+33
Email
pierre.martz@chu-dijon.fr
Facility Information:
Facility Name
Chu Dijon Bourgogne
City
Dijon
ZIP/Postal Code
21000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre MARTZ
Phone
0380293307
Ext
+33
Email
pierre.martz@chu-dijon.fr

12. IPD Sharing Statement

Learn more about this trial

Unipolar Versus Bipolar Interlocking in Humeral Shaft Fractures in Adults

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