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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03868696
Acronym
UDiReCT
Enrollment
48
Registered
2019-03-11
Start date
2019-10-07
Completion date
2020-07-06
Last updated
2020-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colles' Fracture, Radius Distal Fracture

Keywords

Ultrasound, Manipulation under anaesthesia, Emergency Department

Brief summary

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

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.

Interventions

PROCEDUREMUA with sham ultrasound

Standard MUA with sham ultrasound

PROCEDUREMUA with active ultrasound

Standard MUA guided by ultrasound

Sponsors

Royal College of Emergency Medicine
CollaboratorOTHER
Royal Devon and Exeter NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

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.

Intervention model description

1:1 randomised stratified by centre

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Participant recruitment rate6 monthsNumber of participants recruited over the duration of the study

Secondary

MeasureTime frameDescription
Data completeness.6 monthsThe reliability and completeness of data proposed to be collected in a future definitive trial. Measured by the proportion of database fields completed by the end of the study

Other

MeasureTime frameDescription
Emergency Department (ED) manipulation under anaesthesia (MUA) failure rate6 monthsThe proportion (%) of cases having undergone surgical fixation of the index fracture after ED MUA, within 6 weeks of injury . This is the proposed outcome for a definitive trial.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026