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Follow up of Patients After a Visit to Tourcoing Emergency Department for an Ankle Sprain

Follow up of Patients After a Visit to Tourcoing Emergency Department for an Ankle Sprain

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04114552
Acronym
CHEVILLE
Enrollment
112
Registered
2019-10-03
Start date
2019-10-15
Completion date
2020-01-07
Last updated
2020-09-21

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

Conditions

Ankle Sprains

Keywords

inversion trauma, Ankle sprain, physical examination, therapy, recurrence

Brief summary

Ankle sprain is very common. In France, its daily incidence is estimated at 6000. It often causes pain, a temporary period of disability and can results in recurrence and chronic ankle instability. Therefore, an early management and follow up treatment is necessary. Now, functional treatment is clinically the treatment strategy of choice for ankle sprain. It is based on rest, ice, compression, elevation and can use a functional support (like an ankle brace). To evaluate gravity and improve management, a clinical assessment delayed between 4 and 5 days post injury is necessary.

Interventions

OTHERquestionnaires

6 weeks after the trauma,during the call, an oral questionnaire will be proposed to collect data on patients' management since they have left the emergency department. After the call, socio-demographic characteristics, trauma mechanism, medics management will be extracted from the patient's medical records

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

Consulted for ankle trauma as primary reason Agreeing to participate in the telephone survey 6 weeks after trauma Affiliation in a social security scheme

Exclusion criteria

Patients deprived of liberty Patients with an unbalanced psychiatric disease If consultation delayed 48 hours due to trauma Patients with fracture Patients with Chopart or Lisfranc injury Pregnant women People who do not speak French

Design outcomes

Primary

MeasureTime frame
Rate of patients who received a five days post injury new clinical assessmentat 6 weeks

Secondary

MeasureTime frameDescription
Oral questionnairesAt 6 weeksThe questionnaire will ask questions around their socio-demographic characteristics, trauma mechanism, medics management since they have left the emergency department.
Rate of patients receiving physiotherapyAt 6 weeks
Rate of patients with recurrenceAt 6 weeks

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026