Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT07094074 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Exploratory Functional Assessment After Lower Limb Amputation: Locomotion, Balance, Energy Performance and Strategies for Adapting to Orthopaedic Devices

Study acronym: AMILOCO
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Recruitment opened Study sites: 0 to 1 · Start date changed from estimate of Sep 2026 to Sep 18, 2026 · Eligibility criteria expanded, about 11 words Show 3 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of Sep 2026 to Sep 18, 2026
    • Eligibility criteria expanded, about 11 words
  2. Notable Primary and study completion dates: Jan 2031 to Jan 2032 Start date: Sep 2025 to Sep 2026v2 Show 1 more changeShow less
    • Start date: Sep 2025 to Sep 2026
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The general aim of this exploratory study is therefore to investigate and quantify the functional capacities of patients with lower limb amputations (transtibial and transfemoral), with no change in their management, and to describe any changes in these capacities. The volunteers included in this study will be testing new equipment, all of which will be CE-marked, and will therefore meet all the safety and performance conditions required for use by these patients (equipment that is likely to be prescribed as standard). These devices could benefit from current technological advances that could improve these patients' functional abilities. They will be chosen and adapted according to the volunteer's activity and current equipment. This is a local project of the CHU Dijon Bourgogne which will take place on the Technological Investigation Platform located at the Centre de Rééducation et de Réadaptation of the CHU Dijon Bourgogne. A maximum of 100 patients will take part in the study, divided into two sub-groups of between 5 and 50 patients, depending on the type of brace worn and the level of amputation. After the inclusion visit, each volunteer will undergo 2 assessment visits (the order of assessment of the devices will depend on randomisation) separated by 3 to 6 weeks. Follow-up is for a maximum of 14 weeks.
Trial Details
NCT Number NCT07094074
Lead Sponsor Centre Hospitalier Universitaire Dijon
Conditions Lower Limb Amputation
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov