Ultrasound Directed Reduction of Colles Type Distal Radial Fractures in ED (UDiReCT)

NCT ID: NCT03868696

Last Updated: 2020-10-12

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

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-07

Study Completion Date

2020-07-06

Brief Summary

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This is a limited two centre randomized controlled feasibility trial towards a larger definitive trial designed to assess whether bed side ultrasound can reduce the rate of surgical fixation following emergency department manipulation of Colles' type wrist fractures. UDiReCT will mirror the proposed design of the definitive trial but will report feasibility data such as recruitment rate, data completeness and reliability of potential definitive trial outcome measures.

Detailed Description

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Wrist fractures are one of the most common fractures encountered in the Emergency Department (ED). These injuries most frequently happen in people who have fallen onto an outstretched hand and can result in deformity ('displacement') of the broken bone. These 'displaced' (Colles' types of distal radial) fractures can result in long term deformity and problems using the wrist. To prevent this, patients with displaced fractures often undergo manipulation of their fractures, to straighten the wrist, using local anaesthetic or sedation techniques in ED before a plaster cast is applied.

Unfortunately, if ED fracture manipulation is inadequate or the position later 'slips', which can occur in the first 1-2 weeks even in cast, then the patient will need to be admitted to hospital for surgical fixation. Local audit data suggests this affects up to a third of these patients and is a significant additional social and economic burden for patients and healthcare services.

Reducing these fractures as precisely as possible might reduce the subsequent need for surgery. However, ED fracture manipulations are typically done 'blind' with check x-rays after casting, making re-manipulation time consuming with prolonged local anaesthetic times or need for re-sedation. Portable, bedside ultrasound is available in most departments and has been used to guide fracture reduction but it is not known how effective this is nor is it in routine use. Providing this evidence would require a large, multi-centre randomized controlled trial (RCT) trial.

This project aims to determine whether such a trial comparing current practice with ultrasound guided reductions is justified and feasible. This will be done by running a feasibility RCT across two United Kingdom (UK) hospital sites to assess recruitment rates and trial procedures. The investigators hope to recruit about 60 patients in 6 months. This trial will include adults' aged 18 years and older, with Colles' type of distal radial fractures requiring manipulation in ED.

Conditions

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Radius Distal Fracture Colles' Fracture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

1:1 randomised stratified by centre
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
Sham ultrasound will be conducted in control group with screen off and facing away from participant.

Active US screen will also be turned away from participant in the US allocated group and no discussion allowed about the image.

Study Groups

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MUA with sham ultrasound

Participants will undergo standard manipulation (MUA) of wrist fracture with sham ultrasound (screen concealed from participants)

Group Type SHAM_COMPARATOR

MUA with sham ultrasound

Intervention Type PROCEDURE

Standard MUA with sham ultrasound

MUA with active ultrasound

Participants will undergo standard manipulation (MUA) of wrist fracture with active ultrasound (screen concealed from participants)

Group Type EXPERIMENTAL

MUA with active ultrasound

Intervention Type PROCEDURE

Standard MUA guided by ultrasound

Interventions

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MUA with sham ultrasound

Standard MUA with sham ultrasound

Intervention Type PROCEDURE

MUA with active ultrasound

Standard MUA guided by ultrasound

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Adults with Colles' type fractures of the distal radius undergoing fracture manipulation in the ED
* UDiReCT Trial trained staff available

Exclusion Criteria

* Age under 18
* Volar displaced (Smith's) type fractures (well established as being unstable and requiring surgical treatment)
* Unable or unwilling to give informed consent
* Unable or unwilling to be followed up (e.g. orthopaedic follow up in another region)
* Major trauma with other injuries and ISS (Injury Severity Score) \>16
* Urgent manipulation required due to neurovascular or skin compromise
* Open fractures or those with associated nerve or tendon involvement (affect functional outcome)
* Prisoners
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Royal College of Emergency Medicine

OTHER

Sponsor Role collaborator

Royal Devon and Exeter NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Emergency Department

Exeter, Devon, United Kingdom

Site Status

Barking, Havering and Redbridge University Hospitals Nhs Trust

London, , United Kingdom

Site Status

Countries

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United Kingdom

References

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Malik H, Wood D, Stone O, Gough A, Taylor G, Knapp KM, Heggs D, Appelboam A. Ultrasound Directed Reduction of Colles' type distal radial fractures in ED (UDiReCT): a feasibility randomised controlled trial. Emerg Med J. 2023 Nov 28;40(12):832-839. doi: 10.1136/emermed-2023-213279.

Reference Type DERIVED
PMID: 37890981 (View on PubMed)

Other Identifiers

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251149

Identifier Type: -

Identifier Source: org_study_id

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