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Compression Stockings in Ankle Sprain

Prospective Randomized Study of Compression Stockings in Ankle Sprain in Adults

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01259752
Acronym
CASED
Enrollment
130
Registered
2010-12-14
Start date
2010-01-31
Completion date
2012-07-31
Last updated
2012-07-31

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

Conditions

Ankle Sprain

Keywords

Trauma, ankle sprain, emergency, compression stocking

Brief summary

This is a multicenter prospective randomized superiority controlled trial comparing leg stockings and standard care to standard care of ankle sprain and testing the hypothesis that compression stockings enable to reduce the median of recovery from ankle sprain by at least 6 days.

Detailed description

Introduction: Ankle sprain is a frequently encountered trauma lesion in emergency departments and is associated with important health expenses. However, appropriate care of this trauma lesion remains a matter of debate. Hypothesis: The tested hypothesis is that compression stockings enable to reduce the median of recovery from ankle sprain by at least 6 days. Main end point: Delay to recovery of normal painless walking, without any analgesic drug consumption. Secondary end points : Pain at rest and during walking using a visual analog pain scale, bimalleolar and middle-feet perimeters, number of days with analgesic drug consumption, observance analysis, patient's tolerance using a visual analog scale, delay to recover sport activities in the subgroup of patients having a regular sport activity. Methods: Multicenter Prospective randomized superiority controlled trial comparing leg stockings and standard care to standard care of ankle sprain. Standard care include the RICE (Rest, Ice, Compression, Elevation) protocol at admission, immobilization with ankle bracing (3 to 6 week duration according to severity and clinical course), recommendation for walking (no weight baring, partial weight bearing, total weight bearing), administration of analgesic drugs. The medical device tested in the present study is class II compressive stockings (compression between 15 and 20 mmHg). Number of patients: With an alpha risk of 5%, a beta risk of 5%, 70 patients should be included in each group to be able to detect a 6 day difference in the delay of recovery, defined as normal painless walking without any analgesic drug consumption, taking into consideration 10% of patients lost during follow up. Criteria for inclusion: Recent (\<48h) ankle sprain without fracture and without other traumatic lesions in adult patients aged between 18 and 55 years. Patients with limb arterial disease, diabetes, or any diseases expected to potentially interfere with recovery of walking, are excluded as well as pregnant women. Study schedule: Inclusion during first visit to the emergency department, then at day 7, 15-21, 30-45, and 90. Phone call interviews are performed to define the more appropriate timing of the visits.

Interventions

compression stockings

OTHERstandard non compressive stockings

standard non compressive stockings

Sponsors

Pierre and Marie Curie University
CollaboratorOTHER
Poitiers University Hospital
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Recent (\<48h) ankle sprain without fracture and without other traumatic lesions in adult patients aged between 18 and 55 years.

Exclusion criteria

* Patients with limb arterial disease, diabetes, or any diseases expected to potentially interfere with recovery of walking, are excluded as well as pregnant women

Design outcomes

Primary

MeasureTime frame
Delay to recovery of normal painless walking, without any analgesic drug consumption.up to 90 days

Secondary

MeasureTime frameDescription
Bimalleolar perimeterat each follow-up visit (D-7, D-15 to 21, D-30 to 45)
Number of days with analgesic drug consumptionat each follow-up visit (D-7, D-15 to 21, D-30 to 45)
Observance analysisat each follow-up visit (D-7, D-15 to 21, D-30 to 45)Number of days actually wearing compression stocking and ankle bracing and taking analgesic drugs
Pain at rest using a visual analog pain scaleat each follow-up visit (D-7, D-15 to 21, D-30 to 45)
Pain during walking using a visual analog pain scaleat each follow-up visit (D-7, D-15 to 21, D-30 to 45)
middle-feet perimeterat each follow-up visit (D-7, D-15 to 21, D-30 to 45)
Delay to recover sport activities in the subgroup of patients having a regular sport activityat each follow-up visit (D-7, D-15 to 21, D-30 to 45) and at the last follow-up visit (D-90)

Countries

France

Outcome results

None listed

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