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

Ankle Sprains Clinical Trial

— CHEVILLE  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04114552
• Other study ID #: RNI_2019_23
• Secondary ID: 2019-A01824-53
• Status: Completed
• Start date: October 15, 2019
• Est. completion date: January 7, 2020

Study information

• Verified date: September 2020
• Source: University Hospital, Lille
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 112
• Est. completion date: January 7, 2020
• Est. primary completion date: January 7, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 15 Years to 55 Years

Eligibility

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

Related Conditions & MeSH terms

• Ankle Injuries
• Ankle Sprains
• Emergencies
• Sprains and Strains

Intervention

Other:
• questionnaires
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

Locations

Country	Name	City	State
France	Ch Tourcoing	Tourcoing

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of patients who received a five days post injury new clinical assessment		at 6 weeks
Secondary	Oral questionnaires	The questionnaire will ask questions around their socio-demographic characteristics, trauma mechanism, medics management since they have left the emergency department.	At 6 weeks
Secondary	Rate of patients receiving physiotherapy		At 6 weeks
Secondary	Rate of patients with recurrence		At 6 weeks