Compression Stockings in Ankle Sprain (CASED)

This study has been completed.
Sponsor:
Collaborators:
Pierre and Marie Curie University
Poitiers University Hospital
Information provided by (Responsible Party):
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01259752
First received: September 23, 2010
Last updated: July 30, 2012
Last verified: June 2010

September 23, 2010
July 30, 2012
January 2010
July 2012   (final data collection date for primary outcome measure)
Delay to recovery of normal painless walking, without any analgesic drug consumption. [ Time Frame: up to 90 days ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01259752 on ClinicalTrials.gov Archive Site
  • 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) ] [ Designated as safety issue: No ]
  • Bimalleolar perimeter [ Time Frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45) ] [ Designated as safety issue: No ]
  • Number of days with analgesic drug consumption [ Time Frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45) ] [ Designated as safety issue: No ]
  • Observance analysis [ Time Frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45) ] [ Designated as safety issue: No ]
    Number of days actually wearing compression stocking and ankle bracing and taking analgesic drugs
  • 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) ] [ Designated as safety issue: No ]
  • 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) ] [ Designated as safety issue: No ]
  • middle-feet perimeter [ Time Frame: at each follow-up visit (D-7, D-15 to 21, D-30 to 45) ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Compression Stockings in Ankle Sprain
Prospective Randomized Study of Compression Stockings in Ankle Sprain in Adults

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.

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.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Ankle Sprain
  • Device: compression stockings
    compression stockings
    Other Name: compression stockings
  • Other: standard non compressive stockings
    standard non compressive stockings
    Other Name: standard non compressive stockings
  • Experimental: compression stockings
    Intervention: Device: compression stockings
  • Placebo Comparator: standard non compressive stockings
    Intervention: Other: standard non compressive stockings
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
130
July 2012
July 2012   (final data collection date for primary outcome measure)

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
Both
18 Years to 55 Years
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT01259752
P080603
Yes
Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
  • Pierre and Marie Curie University
  • Poitiers University Hospital
Principal Investigator: Pierre Hausfater, MD, PhD Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
June 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP