{"denomUnitsSelected":"Participants","description":"Compliance with treatment was to be measured between both arms of the study. Due to poor accrual (2 participants) and study closure, data was not collected and analysis was not done. There are no results to report due to the limited number of participants.","reportingStatus":"NOT_POSTED","timeFrame":"From registration to study discontinuation. A maximum of 7 months.","title":"Compliance With Treatment as Assessed by the Number of Days Per Week Using MLD or Flexitouch System and Duration/Day of MLD and Flexitouch System Treatment","type":"SECONDARY"}