Comparing New Prothesis PROPRIO-FOOT® Versus Usual Prothesis Tasks Tibial Amputees

Comparaison du Pied Bionique Proprio-Foot® Versus le Pied Habituel Chez Les amputés Tibiaux

Status

Completed

Phases

Phase 4

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02501408

Acronym

PROPRIO-FOOT

Enrollment

Registered

2015-07-17

Start date

2015-03-09

Completion date

2017-04-12

Last updated

2017-11-01

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

Conditions

Lower Limb Amputation at Ankle (Injury)

Brief summary

Evaluate a new porosthetic device in lower limb amputees.

Detailed description

Randomisation between usual and new prosthesis Cross over study of walking performance and VO2 on treadmill with the two devices after 1 month adaptation to each system.

Interventions

DEVICEpropriofoot prosthesis

Adaptation of the device and evaluation after 1 month at home using the studied device

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Tibial amputation * Ability top walk on treadmill * Stable prosthesis for at least 3 months

Exclusion criteria

* Bilateral amputation * Cancer * Absence of consent

Design outcomes

Primary

Measure	Time frame	Description
oxygen consumption	1 mois after adpatation of the selected device	Measurement on treadmill

Countries

France

Outcome results

None listed

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