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CompletedNCT07912476OttawaUpdated Nov 3, 2026

Electronic Decision Support for Ankle Injury X-Ray Assessment

An interventional study of Electronic Clinical Decision Support Alert in Ankle Injuries, Ankle Sprains and Ankle Fractures, sponsored by SPECHBACH Hervé. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-03.

Primary conditionAnkle FracturesRegistry: Ankle InjuriesReclassifiedWhy we changed it
Registry
Ankle Injuries — the first condition term the registry derived for this study.
ClinicalTrials.gg
Ankle Fractures
Why
  1. The study's listed conditions name Ankle Fractures, a narrower term within Ankle Injuries.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by SPECHBACH Hervé · Not applicable, Interventional, and Health services research

From the registry’s dates

  • Registered 4 years 11 months after the study started (first participant enrolled Nov 2021, registered Oct 2026).
Updated Nov 3, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
312
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

Ankle injuries are a common reason for emergency department visits. Although fractures are relatively uncommon, ankle and foot X-rays are frequently ordered to exclude them. The Ottawa Ankle Rules are clinical decision rules designed to help healthcare professionals identify patients who require radiographic imaging. This study evaluated whether an electronic pop-up reminder of the Ottawa Ankle Rules could reduce the number of ankle and foot X-rays prescribed in the emergency department. The study also assessed adherence to the Ottawa Ankle Rules and evaluated their diagnostic performance for identifying fractures.

Read the detailed description

Ankle injuries are a frequent cause of emergency department consultations and often result in radiographic examinations. Despite the low prevalence of fractures, many patients undergo ankle or foot X-rays, leading to unnecessary radiation exposure, increased waiting times, and additional healthcare costs. The Ottawa Ankle Rules (OAR) were developed as a clinical decision aid to safely reduce unnecessary imaging while maintaining a high sensitivity for fracture detection.

This before-and-after study evaluated the impact of an electronic clinical decision support intervention consisting of a pop-up alert reminding physicians of the Ottawa Ankle Rules when ordering imaging for ankle injuries in the emergency department. During the pre-intervention period, physicians followed standard clinical practice. During the intervention period, the electronic reminder was available during the imaging ordering process.

The primary objective was to assess the proportion of patients presenting to the emergency department with ankle trauma who underwent radiographic examination before and after implementation of the electronic alert. Secondary objectives included assessing and comparing the proportion of prescribed X-rays that met Ottawa Ankle Rules criteria before and after implementation of the intervention. The diagnostic performance of the Ottawa Ankle Rules was also evaluated by calculating sensitivity, specificity, and negative predictive value for fracture identification.

02

Conditions studied

  • Ankle Injuries
  • Ankle Sprains
  • Ankle Fractures

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Keywords

  • Ottawa Ankle Rules
  • Clinical Decision Support
  • Electronic Alert
  • Emergency Department
  • Radiography
03

In context

Ankle Fractures Reclassified

202 studies on the registry are indexed under Ankle Fractures; 44 are open to participants now.

This study's enrollment of 312 is above the median of 90 across 150 interventional studies indexed under Ankle Fractures.

Browse Ankle Fractures studies →

Lead sponsor

This is the only study on the registry with SPECHBACH Hervé as lead sponsor.

Compared within Ankle Fractures, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Ankle Injuries. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult patients aged 18 years or older.
  • Presentation to the Emergency Department of Geneva University Hospitals with ankle trauma.
  • Presentation during the study period from 1 November 2021 to 30 April 2022.

Exclusion criteria

Exclusion Criteria:

  • Deep or superficial wounds.
  • Burns.
  • Nerve injury.
  • Vascular injury.
  • Presence of foreign bodies.
  • Animal or insect bites.
  • Gross deformity or dislocation of the foot or ankle.
  • Polytrauma.
  • Unconscious patients.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
312 participants (actual)

Study arms

  • No intervention
    Standard Practice (Pre-Intervention)

    Patients presenting with ankle trauma to the Emergency Department between 1 November 2021 and 31 January 2022. Physicians followed standard routine practice without an electronic clinical decision support alert based on the Ottawa Ankle Rules.

  • Experimental
    Electronic Alert Intervention (Post-Intervention)

    Patients presenting with ankle trauma to the Emergency Department between 1 February 2022 and 30 April 2022. Physicians were exposed to an electronic clinical decision support pop-up alert reminding them to apply the Ottawa Ankle Rules when assessing ankle injuries and ordering imaging.

    Behavioral: Electronic Clinical Decision Support Alert

Interventions

  • BehavioralElectronic Clinical Decision Support Alert

    An electronic clinical decision support pop-up alert integrated into the emergency department workflow. The alert reminded physicians to apply the Ottawa Ankle Rules when evaluating patients with ankle trauma and when considering ankle or foot radiography. The intervention was implemented during the post-intervention period (1 February 2022 to 30 April 2022) and was intended to reduce unnecessary imaging while maintaining appropriate fracture detection

06

What researchers measure

Primary outcomes

  1. Proportion of Patients Receiving Ankle or Foot Radiography

    Assessment of the proportion of patients presenting to the emergency department with ankle trauma who underwent ankle or foot radiography before and after implementation of the electronic clinical decision support alert based on the Ottawa Ankle Rules.

    Time frame: During the emergency department visit (up to 1 day)

Secondary outcomes

  1. Proportion of Radiographs Meeting Ottawa Ankle Rules Criteria

    Proportion of prescribed ankle and foot radiographs that met Ottawa Ankle Rules criteria before and after implementation of the electronic clinical decision support alert.

    Time frame: During the emergency department visit (up to 1 day)

  2. Sensitivity of the Ottawa Ankle Rules for Fracture Detection

    Diagnostic sensitivity of the Ottawa Ankle Rules for identifying fractures among patients presenting with ankle trauma.

    Time frame: Up to 2 weeks after the emergency department visit

  3. Specificity and Negative Predictive Value of the Ottawa Ankle Rules

    Diagnostic specificity and negative predictive value of the Ottawa Ankle Rules for excluding fractures among patients presenting with ankle trauma.

    Time frame: Up to 2 weeks after the emergency department visit

07

Study locations

1 site
  • HUG
    Geneva, Switzerland
08

References and documents

Individual participant data

Plan to share: Yes

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Nov 2021 to primary completion in Apr 2022, 5 months.

Of 69 non-industry interventional studies with no phase under Ankle Fractures, half reached primary completion within 44 months of starting (the median), counting those still running; a quarter within 23 and three quarters within 61. This study's 5 months is below that.

Counting every sponsor, half of 72 studies reached it within 45 months; a quarter within 23 and three quarters within 61.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 12, 2026
First posted
Nov 3, 2026
StartActual
Nov 1, 2021
Primary completionActual
Apr 30, 2022
CompletionActual
Apr 30, 2022
Last update
Nov 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07912476
Lead sponsor
SPECHBACH Hervé
Responsible party
SPECHBACH Hervé (Associate Chief Physician Outpatient Emergency Unit, Primary Care Department, Geneva University Hospitals, University Hospital, Geneva) — Sponsor-investigator
First posted
Nov 3, 2026
Start date
Nov 1, 2021
Primary completion
Apr 30, 2022
Completion
Apr 30, 2022
Last update
Nov 3, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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