Skip to main content
OpenTrials
Completed

NCT Number: NCT01259752

Compression Stockings in Ankle Sprain

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Pitié Salpetriere hospital

Paris, 75013, France

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

compression stockings

Device

compression stockings

standard non compressive stockings

Other

standard non compressive stockings

Primary outcomes

  1. Delay to recovery of normal painless walking, without any analgesic drug consumption.

    Time frame: up to 90 days

Secondary outcomes

  1. Pain at rest using a visual analog pain scale

    Time frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45)

  2. Bimalleolar perimeter

    Time frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45)

  3. Number of days with analgesic drug consumption

    Time frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45)

  4. Observance analysis

    Time frame: at 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

  5. Delay to recover sport activities in the subgroup of patients having a regular sport activity

    Time frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45) and at the last follow-up visit (D-90)

  6. Pain during walking using a visual analog pain scale

    Time frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45)

  7. middle-feet perimeter

    Time frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45)

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • Pierre and Marie Curie University
  • Poitiers University Hospital

Registry information

Official study title

Prospective Randomized Study of Compression Stockings in Ankle Sprain in Adults

Acronym: CASED

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Dec 14, 2010
Registry last updated
Jul 31, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.