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

NCT ID: NCT04114552

Last Updated: 2020-09-21

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

Total Enrollment

112 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-15

Study Completion Date

2020-01-07

Brief Summary

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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.

Detailed Description

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Conditions

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Ankle Sprains

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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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

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

15 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Lille

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Hacène MOUSSOUNI, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Lille

Locations

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Ch Tourcoing

Tourcoing, , France

Site Status

Countries

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France

Other Identifiers

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2019-A01824-53

Identifier Type: OTHER

Identifier Source: secondary_id

RNI_2019_23

Identifier Type: -

Identifier Source: org_study_id

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